HAAG-STREIT

BP 900 Instructions for Use 10 Edition

Instructions for Use

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File Name: HAAG-STREIT - 1500.7220590‑04100 - BP 900 Instructions for Use 10 Edition - 2023-01.pdf

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INSTRUCTIONS FOR USE Slit lamp

BP 900¨ 10. Edition / 2023– 01

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INSTRUCTIONS FOR USE Slit lamp

BP 900¨ 10. Edition / 2023– 01

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Preface Thank you for choosing a Haag-Streit device. Provided you comply carefully with the regulations in these instructions for use, we can guarantee reliable and trouble-free use of our product. WARNING! Read the instruction manual carefully before commissioning this product. It contains important information regarding the safety of the user and patient. NOTE! For USA only: Federal law restricts this device to sale by or on the order of a physician or licensed practitioner. WARNING! This device is equipped with high intensity light emitting diodes. Excessive exposure of patients in treatment with certain medication may lead to phototoxic adverse reactions, due to higher photosensitivity.

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Contents ¥

1 Safety ...4 ◦ ◦ ◦ ◦ ◦ ◦ ◦ ◦ ◦ ◦

1.1 Comments on these instructions for use...4 1.2 Ambient conditions...4 1.3 Shipment and unpacking ...4 1.4 Installation warnings ...4 1.5 Operation, environment ...5 1.6 Light toxicity ...5 1.7 Disinfection ...6 1.8 Warranty and product liability ...6 1.9 Reporting obligation ...6 1.10 Description of symbols...6

2 Intended purpose / intended use ...6 ◦

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2.1 Device description...6 ▪ 2.1.1 Intended users ...7 2.2 Medical purpose...7 ▪ 2.2.1 Indications...7 ▪ 2.2.2 Part of the body ...7 ▪ 2.2.3 Patient population ...7 ▪ 2.2.4 Contraindications ...7 2.3 Principles of operation ...7 ▪ 2.3.1 Operating environment ...7 2.4 Clinical benefit...7

3 Introduction ...8

4 Device assembly / installation ...9

5 Commissioning ...9

6 Operation...10

¥ ¥

7 Decommissioning ...12 8 Technical data ...13

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8.1 Slit illumination... 13 8.2 Stereo microscope... 13 8.3 Instrument base... 13 8.4 Dimensions... 13

9 Maintenance ... 14

10 Appendix ... 15

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9.1 Device inspection ... 14 9.2 Servicing... 14 9.3 Cleaning and disinfection ... 14 9.4 Replacing the illumination mirror ... 14 9.5 Dust cover ... 14

10.1 Accessories / functionals parts / detachable parts / consumables ... 15 10.2 Legal regulations ... 15 10.3 Classification ... 15 10.4 Disposal... 16 10.5 Observed standards ... 16 10.6 Information and manufacturer's declaration concerning electromagnetic compatibility (EMC) . 16 ▪ 10.6.1 General... 16 ▪ 10.6.2 Emitted interference ... 17 ▪ 10.6.3 Electromagnetic immunity environment tested (part 1) ... 18 ▪ 10.6.4 Electromagnetic immunity environment tested (part 2) ... 19 ▪ 10.6.5 Recommended separation distances between portable and mobile RF communications equipment and this product ... 21

3.1 Overview ...8 4.1 Microscope and illumination...9 4.2 Power supply ...9 4.3 Instrument base with weight compensation facility ...9 4.4 Setting the weight compensation facility ...9 4.5 Switching on the compensation facility ...9 4.6 Switching off the compensation facility ...9 4.7 Regulating the clearance of the slit width controls...9 5.1 Switching on the device ...9

6.1 Setting the eyepieces...10 6.2 Preparing the patient...10 6.3 Operating the device...10 6.4 Setting the filters & diaphragms ...12 6.5 Fixation star ...12 6.6 Microscope and eyepiece ...12

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1 Safety

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1.3 Shipment and unpacking

DANGER! Failure to comply with these instructions may result in material damage or pose a danger to patients or users. WARNING! These warnings must absolutely be complied with to guarantee safe operation of the product and to avoid any danger to users and to patients. NOTE! Important information, please read carefully.

1.1 Comments on these instructions for use NOTE! In these instructions for use the point is used as decimal separator.

• • • • • • • • •

Before unpacking the device, check whether the packaging shows traces of improper handling or damage. If this is the case, notify the transport company that delivered the goods to you. Unpack the device together with a representative of the transport company. Make a report of any damaged parts. This report must be signed by you and by the representative of the transport company. Leave the device in the packaging for a few hours before unpacking it (condensation). Check the device for damage after it is unpacked. Return defective devices in the appropriate packaging. Store packaging material carefully so that it can be used for potential returns or when moving. The slit lamp and headrest must be installed on an electrically insulated, fireproof table top. The rail covers (a) prevent the slit lamp from tilting. Check that the connection parts of the accessories are in the correct position (screw connections, quick-release fasteners).

1.2 Ambient conditions Transport

Temperature

−40 °C ... +70 °C

Air pressure

500 hPa ... 1060 hPa

Relative humidity Storage

Temperature

−10 °C ... +55 °C

Air pressure

700 hPa ... 1060 hPa

Relative humidity Use

10 % ... 95 %

Temperature

+10 °C ... +35 °C

Air pressure

800 hPa ... 1060 hPa

Relative humidity

10 % ... 95 %

30 % ... 90 %

1.4 Installation warnings WARNING! • Do not modify this device without authorization of the manufacturer. Installation and repairs may only be performed by trained specialists. • Any third-party device must be connected in compliance with the EN 60601-1 standard. • Only original Haag-Streit spare parts may be used. • Use of this device adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If

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such use is necessary, this device and the other equipment should be observed to verify that they are operating normally. • Grounding reliability can only be achieved when unit is connected to a hospital grade receptacle. (Not valid for EU countries). • The device should be set up in such a way that the plug is always easily accessible and the device can easily be disconnected from the mains.

1.5 Operation, environment DANGER! Never use the device in potentially explosive environments where volatile solvents (alcohol, petrol, etc.) and flammable anaesthetics are in use. WARNING! • The device must be switched off after every use. Otherwise there is a risk of overheating when a protective dust cover is used. • This device must not be operated near of high frequency surgical equipment and the radio frequency shielded room of a medical electrical system for magnetic resonance imaging, where the intensity of electromagnetic disturbances is high. • Portable radio frequency communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the device, including cables specified by Haag-Streit. Otherwise, degradation of the performance of this device could result. NOTE! • This device must only be operated by qualified personnel. The owner is responsible for their training. • This device may only be used in accordance with the instructions in the 'Intended purpose / intended use' chapter.

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1.6 Light toxicity WARNING! • The light emitted from this device is potentially hazardous. The longer the duration of exposure, the greater the risk of ocular damage. Exposure to light from this device when operated at maximum intensity will exceed the safety guideline after 131 seconds. (EN ISO 15004-2) • For USA only: The light emitted from this device is potentially hazardous. The longer the duration of exposure, the greater the risk of ocular damage. Exposure to light from this device when operated at maximum intensity will exceed the recommended maximum exposure (RME) of 2.2 J/cm² after 28 seconds. Caution is generally advised when exposing a patient to light radiation. However, because of a significant risk of injury at exposures exceeding 10 J/cm², the user should avoid exposures longer than 131 seconds. (ANSI Z80.36) • For USA only: The emissions of this device can exceed the specified limits for "weighted retinal visible and infrared radiation thermal irradiance" (EVIR-R) defined in ANSI Z80.36. The device operates within the defined limits when the slit width is kept under 2 mm. • As extended, intensive illumination can damage the retina, the use of the device in the examination of the eye should not be prolonged unnecessarily. The illumination of this slit lamp emits a radiation in the range between 400 and 750 nm. Detailed information on the radiation can be provided on request. • The retinal dose for a photochemical risk is composed of the product of the radiance and the exposure time. If the radiance is halved, the time until the exposure time limit value is reached will double accordingly. To date, no acute, optical radiation hazard has been detected in slit lamps. Nevertheless, we recommend keeping the intensity of the light reaching the patient's retina to the minimum possible for the respective diagnosis. Children, people with aphakia and people suffering from eye conditions are most at risk. An increased risk may also occur if the retina is exposed to the same or a similar device with a visible light source within 24 hours. This applies, in particular, if the retina has been photographed with a flashbulb in advance.

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1.7 Disinfection NOTE! The device can, but does not need to be disinfected. For more information, please refer to the 'Maintenance' chapter.

1.8 Warranty and product liability •

Haag-Streit products must be used only for the purposes and in the manner described in the documents distributed with the product. • The product must be treated as described in the ‘Safety’ chapter. Improper handling can damage the product. This would void all guarantee claims. • Continued use of a product damaged by incorrect handling may lead to personal injury. In such a case, the manufacturer will not accept any liability. • Haag-Streit does not grant any warranties, either expressed or implied, including implied warranties of merchantability or fitness for a particular use. • Haag-Streit expressly disclaims liability for incidental or consequential damage resulting from the use of the product. • This product is covered by a limited warranty granted by your seller. • For USA only: This product is covered by a limited warranty, which may be reviewed at www.haag-streit-usa.com.

1.9 Reporting obligation NOTE! Any serious incident that has occurred in relation to the device must be reported to Haag-Streit and the competent authority of the Member State in your country.

1.10 Description of symbols

Follow instruction for use

Read the instructions for use attentively

General warning, read the accompanying documentation

European certificate of conformity

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Date of manufacture

Manufacturer

Haag-Streit reference number

Serial number

Trademark of the manufacturer Haag-Streit AG

Notes on disposal, see the 'Disposal' chapter

Listed European Authorized Representative

Medical Device

Testsymbol of TÜV Rheinland with approval for INMETRO Brasil

MET Listed Mark with approval for USA and Canada

2 Intended purpose / intended use A slit lamp biomicroscope is intended for use in eye examination. It is used to aid in the diagnosis and documentation of diseases or trauma which affect the structural properties of the eye.

2.1 Device description The devices of the slit lamp are made up of: • • • •

Stereo biomicroscope Slit illumination Instrument base Headrest and chin rest

The illumination system and a biomicroscope are mounted to an instrument base operated by joystick. The single joystick allows horizontal and vertical displacement of the slit lamp across the examination table. Both elements, the illumination system and the biomicroscope, can be swiveled progressively across the pivot, independently of one another. A sturdy headrest is attached to the table. Both the table and the chin rest are adjustable in height to provide a comfortable, yet sturdy examination position to the patient, outside of the device's range of motion. As this device operates non-invasively it only comes into contact with the patient at the chin rest and forehead band.

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2.1.1 Intended users

•

Users are qualified medical professionals such as ophthalmologists, optometrists, opticians, nurses and researchers or other qualified specialists as permitted by local legislation.

• •

2.2 Medical purpose

•

This device has the following medical purpose: • • •

Diagnosis and monitoring of diseases of the anterior segment of the eye Diagnosis and monitoring of injuries of the anterior segment of the eye Investigation of the anatomy and physiological or pathological state of the anterior segment of the eye

2.2.1 Indications The use of the slit lamp is indicated for the following medical conditions: • • • • •

Local and systemic diseases affecting the eye Lesions and defects of the anterior segment Acute infections and inflammations Presence of intraocular foreign bodies Other traumata of the eye

2.2.2 Part of the body The slit lamp is intended for the examination of the human eye, specifically the anterior segment of the eye (i.e., lids, lashes, conjunctiva, cornea, anterior chamber, iris, and lens).

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The microscope arm and the illumination arm are mounted on an instrument base: Both can be swivelled independently around the same vertical axis. The instrument base can be moved in all three axes. When illuminating transparent media with a narrow, sharp slit, an 'optical section' can be magnified and viewed through the microscope. The patient's head is fixed to a height-adjustable headrest holder so that the examination can be carried out quickly and as comfortably as possible for both doctor and patient.

2.3.1 Operating environment The slit lamp is intended to be used in professional health care facilities such as hospitals, physician's, optometrist's and optician's practices. For optimal use of the slit lamp, the ambient lighting should be attenuated to improve image contrast. In case of transillumination of the iris or for viewing details at great magnification at a narrow slit, it may be necessary to completely darken the room.

2.4 Clinical benefit The use of the slit lamp allows for the systematic examination of the eye under magnification, thus permitting the diagnoses of pathologies that may have otherwise remained unidentified and could have lead to blindness if left untreated. The clinical benefits of the product outweigh the remaining residual risks to the patient.

2.2.3 Patient population This device is intended for use on human patients with the physical ability to sit in front of a slit lamp with their head resting against the headrest in a steady position and the mental ability to follow instructions.

2.2.4 Contraindications There are no known contraindications.

2.3 Principles of operation •

The slit lamp implements the principle of focal illumination: The focal point of the microscope and the illumination coincide.

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3 Introduction The slit lamp consists of an illumination and a binocular microscope. The instrument base can be used to move the entire device in front of the eyes. The illumination offers a large number of setting options to make the practically invisible areas in the eye visible. There is also a range of accessories available for the slit lamp to allow special diagnosis possibilities in addition to the general examinations.

3.1 Overview 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 19.

Lamp cable Headrest Headband Height mark on headrest (patient eye) Adjustable fixation lamp Chin rest Height adjustment of chin rest LED illumination LI 900, see separate manual Background illumination (fixed) Lever for filters Scale for angled position of the slit image (5° increments) Background illumination with swivel bracket Illumination mirror Diffusor Magnification changer Mounting screw for the stereo microscope Slot for accessories (test rod, background illumination, etc.) Centring screw Illumination unit / microscope angle scale

20. 21. 22. 23. 24. 25. 26. 27. 28. 29. 30. 31. 32. 33. 34. 35. 36. 37. 38. 39. 40.

Illumination arm locking screw Slit width controls Microscope arm locking screw Cross slides Rail cover Illumination control 'on table' Illumination control 'in table' Slit length / diaphragm scale Slit length, slit rotation, blue filter and fixation star control Cover screw for accessories pin Quick-release fastener for accessories Stereo microscope Eyepieces Thread for fixing the tonometer AT 900 mod. BP or tonometer AT 900 D mod. BP Mounting screw for breath shield Breath shield Inclination angle latch 5 – 20° Joy stick base locking screw Axle Control lever Slide plate

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4 Device assembly / installation WARNING! • Do not modify this device without authorization of the manufacturer. Installation and repairs may only be performed by trained specialists. • Contact your Haag-Streit representative for installation, repairs and modification work on the system. The contact details are available at www.haag-streit.com. • Only original Haag-Streit spare parts may be used.

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4.5 Switching on the compensation facility Turn anticlockwise until the screws (59) are completely released.

4.6 Switching off the compensation facility Turn clockwise until you meet resistance. Verify whether the microscope arm springs back downwards if you push it upwards with your hand. This will only happen if the load is already at maximum. Generally, as many counterbalance springs should be deactivated as necessary until this spring action occurs. The weight compensation facility is set correctly once the illumination and microscope with the mounted accessories weigh slightly more than the counterbalance springs.

4.1 Microscope and illumination

4.7 Regulating the clearance of the slit width controls

•

The small screw in the centre of the right control knob (83) allows you to regulate the friction of the turning movement of these adjusting knobs. Turning it slightly to the right (in) makes it harder, turning it left (out) makes it easier. It should at least be set so hard that the slit cannot close on its own.

•

The slit lamp is packaged and delivered fully assembled. The transport safety devices must be removed prior to commissioning. Fix the breath shield (35) in place by fastening the knurled screw (34) on the inside of the bearer arm.

4.2 Power supply NOTE! • Observe the respective Haag-Streit instructions for use. For further information, please contact your Haag-Streit representative. • This device must only be operated with PS-LED and PS-LED HSM 901 Haag-Streit power supplies and the RM02 release module.

4.3 Instrument base with weight compensation facility The weight of additional accessories mounted on the microscope can be compensated using counterbalance springs. This keeps the height adjustment of the slit lamp easy.

4.4 Setting the weight compensation facility Turn the control lever (60) to its lowest position and then loosen it slightly a quarter turn. Turn the microscope and illumination to the side. Apply 1−3 springs depending on the accessory.

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5 Commissioning

The device can be switched on and off using the mains power switch on the power supply. The green lamp in the rocker switch lights up when the device is switched on.

5.1 Switching on the device • •

Connect the power supply to the mains and press the rocker switch. The green lamp in the rocker switch lights up when the device is switched on. Turn the rotating knob on the illumination control to a position between '1' and '10'.

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6 Operation

•

6.1 Setting the eyepieces

•

NOTE! The eyepieces must be individually set prior to the first examination in accordance with the refraction of the examiner. Insert the provided focus test rod (41) in place of the protective cover (42) and turn its black projection surface at a right angle to the microscope axis. Return the illumination and microscope to the central position (0°).

41. Test rod 42. Protective cover 43. Sliding occluders

• •

• • • •

Each eyepiece should be set individually by turning the knurled ocular refraction ring with dioptre scale until the projected slit can be seen in focus. The setting is performed from the (+) to the (-) side at low magnification. The required pupil distance should then be set on the microscope. The sliding occluders (43) are used to set the correct working distance for the examiner from the eyepiece. Examiners who do not wear glasses: Pull the occluders out as far as they will go. Examiners who do wear glasses: Push the occluders in as far as they will go.

6.2 Preparing the patient • •

In order to attain a solid basis for the forehead and chin to rest on, the table height should be selected such that the patient sits bent over forward. To ensure that only the part of the eye being examined is illuminated, the slit height should be set accordingly in order to avoid distracting streaking of light.

Applied parts which come into contact with the patient (headrest) should be disinfected prior to every use (see instructions for use 'Headrest'). The slit lamp must be switched off after every examination in accordance with the 'Decommissioning' chapter.

WARNING! The device must be switched off after every use. Otherwise there is a risk of overheating when a protective dust cover is employed.

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6.3 Operating the device

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Use the turn screw (7) to set the chin rest (6) in such a way that the patient’s eyes are at the same height as the black mark (4) on the sides of the headrest. Adjust the eyepieces (32) in accordance with the examiner’s refraction by turning the knurled rings and set the eye distance. Switch on the illumination by turning the switch on the power supply. Adjust the height of the slit lamp by turning the control lever (39) until the light beam and microscope axis are at eye level. The magnification of the stereo microscope is changed using the magnification changer (15). The rigid control lever (40) gently inclined towards the examiner can be used to push the entire device until the slit appears approximately focused on the cornea. This initial setting is verified with the naked eye. Fine tuning is performed by tilting the control lever while observing via the stereo microscope (31). The slit width is set left or right with the rotating knob (21), as is the angle between the stereo microscope and illumination. The slit image can be set vertically, horizontally or as diagonal as required by turning the illumination facility on the handle (28) (locking points at 45°, 90° and 135°; stops at 0° and 180°; scale in 5° increments). To ensure that unimpeded binocular fundus examination is also possible at lateral angles of between 3° and 10°, a short mirror (13) is used, the illumination turned 90° using the locking screw (21) and tilted in 5° steps using the latch (36), and the illumination and microscope turned to the central position (0°). Front lenses and contact lenses are used to examine the ocular fundus.

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Diffuse illumination: •

Connecting the diffusor (14) upstream creates diffused illumination. This allows monitoring of the overview and can be used to capture the overview with an imaging module.

Indirect illumination: •

For observation in regredient light (indirect illumination), the centring screw (18) is loosened in order to move the slit image out of the centre of the visual field. Tightening the screw centres the slit image again.

Slit tilting: •

The latch (36) can be used to tilt the illumination in 5° steps. This creates an angled light beam during horizontal slit orientation. Tilting the slit enables reflexfree examination with contact lenses (fundus and gonioscopy) and magnifying lenses.

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6.4 Setting the filters & diaphragms a. b. c. d. e. f. g. h.

Open Grey filter (10%) Red removal filter Reserve opening for filter of choice ø 15 mm (0 / –0.2), thickness 2.5 mm Fixation star (predominantly used for fixation examination of cross-eyed children with amblyopia) Apertures of ø 8, 5, 3, 2, 1 and 0.2 mm Display of slit length adjustment from 1 to 14 mm Blue filter

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6.6 Microscope and eyepiece 44 45 46 44. Frontal objective f 103 mm 45. Rotary knob displaying the set magnification 46. 3-level magnification changer (Galilei system) 47. Quick-release fastener for knurled ring 48. Binocular tube f 130 mm with convergent insight, pupil distance can be set from 52 − 78 mm 49. Eyepiece 12.5 × / field of vision ø 16 mm 50. Index (white point) 51. Knurled ring with dioptre scale for setting the refraction of the examiner (± 6 D) 52. Sliding occluder (for people who wear glasses)

47 48 49 50 51 52

7 Decommissioning 6.5 Fixation star •

•

Turning the diaphragm disc as far as it will go to the left switches on the fixation star and the symbol "S" appears in the window. In some examinations of the fundus, this star is projected onto the ocular fundus and is also visible to the patient, who is asked to focus on the centre hole of the star. This allows the examiner to see where the patient's vision is most focused. A typical use of the fixation star is during laser treatments close to the macula. Similarly, it is also possible to identify microstrabismus with the projection of the fixation star. The fixation star is usually used with an upstream red removal filter.

The LED illumination can be switched off with the illumination controls. The power supply remains switched on during this process and the switch lights up green. To switch the system off completely, the rocker switch must be set to the 0 = 'OFF' position. This creates a two-pole isolation from the mains. NOTE! Disconnect the power supply from the mains if you do not intend to use it for an extended period of time.

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8 Technical data

8.2 Stereo microscope

8.1 Slit illumination

Stereo angle:

13°

Magnification changer:

10× / 16× / 25×

Ocular magnification:

12.5×

Range of adjusting eye-pieces:

+6 to −6 dioptres 53 – 78 mm

NOTE! Detailed information regarding the radiation can be provided on request. Spectral range slit illumination

400 to 750 nm

Pupil distance:

Spectral range background illumination

400 to 750 nm

Total magnification:

10× / 16× / 25×

Slit image width

0 – 14 mm continuous

Object field ø in mm:

20.0 / 12.7 / 8.0

Slit image length

1 – 14 mm continuous

Illumination field circle

ø 8 / 5 / 3 / 2 / 1 / 0.2 mm

8.3 Instrument base

Test mark

With fixation star

Slit image rotatability

± 90°

Swiveling of the slit illumination to the microscope axis Filters

Operation:

Single-handed operation of control lever in three dimensions

Horizontal ± 90°, vertical 0 – 20°

Adjustment of instrument base:

100 mm (length) 100 mm (side) 30 mm (height)

Blue, red removal (green), grey (10%)

8.4 Dimensions

NOTE! (Further information available in the LED illumination LI 900 instructions for use)

Weight:

12.3 kg (without power supply, headrest and options)

Dimensions L × W × H:

305 × 332 × 700 mm

Packaging L × W × H:

420 × 510 × 780 mm

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9 Maintenance WARNING! • Do not modify this device without authorization of the manufacturer. Installation and repairs may only be performed by trained specialists. • Contact your Haag-Streit representative for installation, repairs and modification work on the system. The contact details are available at www.haag-streit.com. • Only original Haag-Streit spare parts may be used. The LED illumination can be operated maintenance-free for its entire service life.

9.1 Device inspection In order to correctly check the slit lamp, proceed as follows: • • • • • • • •

Insert the test rod into the radial movement bearing, whilst at the same time aligning the surface to the microscope at a right angle. Set the slit length to 8 or 14 mm. Set the illumination intensity to 50%. Set the magnification in the microscope to max. Set the eyepieces in such a way that the test rod is in sharp focus. In doing so, turn the ocular from the (+) to the (-) side. For all magnifications, the structure of the test rod must be shown in sharp focus. Close the slit edges to approx. 0.5 mm. The edges must be shown in sharp focus. Open the slit edges completely and turn the test rod by 45°, the sharp area must be in the centre of the test rod.

9.2 Servicing To guarantee a long service life, the device must be cleaned weekly as described and protected with the dust cover when not in use. We recommend having the device inspected once a year by an authorized service technician.

9.3 Cleaning and disinfection

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disinfectants (containing aldehyde or aldehyde-free) are also permitted, such as Kohrsolin FF. WARNING! • The preparation instructions provided do not apply to tonometer measuring prisms. • Tonometer measuring prisms must be prepared in accordance with a different manual. • Too strong or aggressive disinfectants or cleaning liquids e.g. hydrogen peroxide will damage the finish and coating of the device. • Do not use sprays. • Observe the manufacturer's safety instructions. • Do not use any cloths that drip. • Wring out any soaked cloths before use when necessary. • Ensure that no liquid penetrates the device. • Comply with the stipulated exposure time. • Clean optical surfaces after disinfection with a very soft cloth. NOTE! IP code: IPX0 (device is not protected against liquids)

9.4 Replacing the illumination mirror The mirror can be most easily accessed if the microscope is turned away from the illumination and the illumination inclined two points. WARNING! Only use mirrors with a LOT number.

9.5 Dust cover We recommend protecting the slit lamp with a dust cover when not in use.

The Haag-Streit slit lamps and their accessories can, if required, be carefully wiped down with ready-for-use disposable 70% ethanol disinfectant wipes. Surface-friendly 14

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10 Appendix WARNING! • Do not modify this device without authorization of the manufacturer. Installation and repairs may only be performed by trained specialists. • Contact your Haag-Streit representative for installation, repairs and modification work on the system. The contact details are available at www.haag-streit.com. • Only original Haag-Streit spare parts may be used.

10.1 Accessories / functionals parts / detachable parts / consumables Components Contrast enhancing filter (yellow) BP 900

REF 1007839

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Diagnostic contact lenses

Please refer to the instructions for use 'Contact lenses, Goldmann/Diagnostics/Laser'

Applanation Tonometer

Please refer to the instructions for use 'Applanation tonometer AT 900 / AT 870' and 'Applanation tonometer AT 900 D'

Headrest

Please refer to the instructions for use 'Headrest'

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10.2 Legal regulations • • • •

Eyepiece 10x with reticule for estimating length and angle (BM900). To 1400265 be used in combination with 7220737 • •

This device was developed and designed taking the EN 60601-1, EN ISO 10939 and EN ISO 15004-2 standards into account. The EN 60601-1 standard must be observed when using different medical and/ or non-medical electrical devices in combination. Compliance of the device with the EU 2017/745 (Medical Device Regulation) is confirmed by the CE-designation. The device satisfies the electromagnetic compatibility requirements of EN 60601-1-2. The device has been designed to maintain the emissions of electromagnetic interference at a level which does not exceed the statutory guidelines and which does not affect other devices in its vicinity. The device also has the immunity stipulated by the standard. You can request a copy of the declaration of conformity for this device from Haag-Streit at any time. Statutory accident regulations are to be observed.

Eyepiece 12.5x for estimating length

1400302

Eyepiece 12.5x with crosshair reticule

3000470

Eyepiece 12.5x with dioptre adjustment

1400303

•

Eyepiece 12.5x with McIntyre comparison grid

1400304

10.3 Classification

Imaging module IM 600 BP

7220539

Breath shield (slit lamp BQ/BM/BP)

1007129

Protection shield large (for BP 900)

7221002

Short mirror

1001591

Fine brush for cleaning the optics

1001398

FRANÇAIS

Standard EN 60601-1

Protection class I

Operating mode

Continuous operation

EU 2017/745 (Medical Device Regulation)

Class I

FDA

Class II

ENGLISH

DEUTSCH

FRANÇAIS

ITALIANO

ESPAÑOL

10.4 Disposal Electrical and electronic devices must be disposed of separately from household waste! This device was made available for sale after the 13th August 2005. For correct disposal, please contact your HaagStreit representative. This will guarantee that no hazardous substances enter the environment and that valuable raw materials are recycled.

10.5 Observed standards EN 60601-1 EN 60601-1-2 EN ISO 10939 EN ISO 15004-2 ANSI Z80.36

PORTUGUÊS

NEDERLANDS

SVENSKA

10.6 Information and manufacturer's declaration concerning electromagnetic compatibility (EMC) 10.6.1 General This device fulfills the requirements on electromagnetic compatibility according to IEC 60601-1-2:2014+A1:2020 (Edition 4.1). The device is built so that the generation and emission of electromagnetic interference is limited to the extent that other devices are not disturbed in their use in accordance with the regulations and so that the device itself is suitably immune to electromagnetic interference. WARNING! • Electrical medical devices and systems are subject to special EMC measures and must be installed in accordance with the EMC instructions contained in this accompanying document. • Use of accessories, transducers and cables other than those specified or provided by Haag-Streit could result in increased electromagnetic emissions or decreased electromagnetic immunity of this device and result in improper operation. • Third-party devices may only be connected in compliance with the IEC 60601-1 standard.

SVENSKA

NEDERLANDS

PORTUGUÊS

ESPAÑOL

ITALIANO

FRANÇAIS

DEUTSCH

ENGLISH

10.6.2 Emitted interference This product is intended for use in the electromagnetic environment specified below. The customer or the user of this product should assure that it is used in such an environment. Emission test

Compliance

Electromagnetic environment - guidance

RF emissions CISPR 11

Group 1

This product uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

RF emissions CISPR 11

Class B

Harmonics emissions IEC 61000-3-2

Not applicable

This product is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.

Voltage fluctuations/flicker emissions IEC 61000-3-3

Not applicable

ENGLISH

DEUTSCH

FRANÇAIS

ITALIANO

ESPAÑOL

PORTUGUÊS

NEDERLANDS

SVENSKA

10.6.3 Electromagnetic immunity environment tested (part 1) This product is intended for use in the electromagnetic environment specified below. The customer or the user of this product should assure that it is used in such an environment. Immunity test

IEC 60601 test level

Compliance level

Electromagnetic environment Ð guidance

Electrostatic discharge (ESD) IEC 61000-4-2

± 8 kV contact ± 2, ± 4, ± 8, ± 15 kV air

Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.

Electrical fast transient/burst IEC 61000-4-4

± 2 kV, 100kHz for power supply lines * ± 2 kV, 100kHz for power supply lines * Mains power quality should be that of a typical com± 1 kV, 100 kHz for input/output lines * ± 0.5, ± 1 kV, 100 kHz for input/output mercial or hospital environment. * Not applicable for DC and I/O if cable < 3 m. lines *

Surge IEC 61000-4-5

± 0.5, ± 1 kV line(s) to line(s) * ± 0.5, ± 1, ± 2 kV line(s) to earth *

± 1 kV line(s) to line(s) * ± 0.5, ± 1, ± 2 kV line(s) to earth *

Voltage dips, short interruptions 0% UT: 0.5 cycle at 0°, 45°, 90°, 135°, 0% UT: 0.5 cycle at 0°, 45°, 90°, 135°, and voltage variations on power 180°, 225°, 270° and 315° 180°, 225°, 270° and 315° supply input lines IEC 61000-4-11 0% UT: 1 cycle at 0° 0% UT: 1 cycle at 0°

Power frequency (50/60 Hz) magnetic field IEC 61000-4-8

0% UT: 250/300 cycles at 0°

70% UT: 25/30 cycles at 0°

3 A/m 50/60 Hz

30 A/m 50/60 Hz

Mains power quality should be that of a typical commercial or hospital environment. * Not applicable for DC and I/O if cable < 3 m. Mains power quality should be that of a typical commercial or hospital environment. If the user of this product requires continued operation during power mains interruptions, it is recommended that this product be powered from an uninterruptible power supply or battery. UT is the a.c. mains voltage (100 – 240 V) prior to application of the test level. Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

SVENSKA

NEDERLANDS

PORTUGUÊS

ESPAÑOL

ITALIANO

FRANÇAIS

DEUTSCH

ENGLISH

10.6.4 Electromagnetic immunity environment tested (part 2) Portable and mobile RF communications equipment should be used no closer to any part of this product, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. Immunity test

IEC 60601 test level

Conducted RF IEC 61000-4-6

3 Vrms 3 Vrms If the measured field strength in the location in which this product 150 kHz – 80 MHz outside ISM 150 kHz – 80 MHz outside ISM is used exceeds the applicable RF compliance level, this product bands and radio amateur band * bands and radio amateur band * should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating this product. 6 Vrms 6 Vrms 150 kHz – 80 MHz in ISM bands 150 kHz – 80 MHz in ISM bands and radio amateur band * and radio amateur band * Minimum separation distance shall be calculated by following equation: 3 V/m 3 V/m 80 MHz – 6 GHz 80 MHz – 2.7 GHz 80% AM 1 kHz 80% AM 1 kHz

Radiated RF IEC 61000-4-3 Proximity field from RF wireless communication equipment IEC 61000-4-3

27 V/m 380 – 390 MHz 50% PM 18 Hz

Compliance level

27 V/m 380 – 390 MHz 50% PM 18 Hz

Electromagnetic environment - guidance

E is the immunity test level in [V/m] d is the minimum separation in [m] P is the maximum power in [W]

28 V/m 28 V/m 430 – 470 MHz 430 – 470 MHz FM ± 5 kHz deviation, 1kHz sine FM ± 5 kHz deviation, 1kHz sine RF wireless equipment maximum output power and separation distance tested (at 30 cm): 9 V/m 9 V/m 704 – 787 MHz 704 – 787 MHz TETRA 400: max 1.8 W 50% PM 217 Hz 50% PM 217 Hz GMRS 460, FRS 460: max 2 W 28 V/m 28 V/m LTE Band 13 and 17: max 0.2 W 800 – 960 MHz 800 – 960 MHz GSM 800/900: max 2 W 50% PM 18 Hz 50% PM 18 Hz TETRA 800: max 2 W 28 V/m 28 V/m iDEN 820: max 2 W 1700 – 1990 MHz 1700 – 1990 MHz CDMA 850: max 2 W 50% PM 217 Hz 50% PM 217 Hz LTE Band 5: max 2 W

ENGLISH

DEUTSCH

FRANÇAIS

ITALIANO

ESPAÑOL

PORTUGUÊS

28 V/m 2400 – 2570 MHz 50% PM 217 Hz

9 V/m 5100 – 5800 MHz 50% PM 217 Hz

Radiated fields in close proximity 8 A/m IEC 61000-4-39 30 kHz

8 A/m 30 kHz

65 A/m 134.2 kHz

65 A/m 134.2 kHz **

7.5 A/m 13.56 MHz

NEDERLANDS

SVENSKA

GSM 1800/1900: max 2 W CDMA 1900: max 2 W DECT: max 2 W LTE Band 1, 3, 4, 25: max 2 W UMTS: max 2 W Bluethooth: max 2 W WLAN 802.11b/g/n: max 2 W RFID 2450: max 2 W LTE Band 7: max 2 W WLAN 802.11 a/n: max 0.2 W Interference may occur in the vicinity of equipment marked with the following symbol:

* The ISM (industrial, scientific and medical) bands between 150 kHz and 80 MHz are: 6.765 – 6.795 MHz, 13.553 – 13.567 MHz, 26.957 – 27.283 MHz, 40.66 – 40.7 MHz. The amateur radio bands between 0.15 MHz and 80 MHz are: 1.8 MHz – 2 MHz, 3.5 – 4.0 MHz, 5.3 – 5.4 MHz, 7 – 7.3 MHz, 10.1 – 10.15 MHz, 14 – 14.2 MHz, 18.07 – 18.17 MHz, 21.0 – 21.4 MHz, 24.89 – 24.99 MHz, 28.0 – 29.7 MHz, 50.0 – 54.0 MHz. ** In the event of a severe 134.2 kHz interference, communication to the illumination head may be lost. It may be necessary to restart the device manually. If the measured field strength in the location in which this product is used exceeds the applicable RF compliance level above, this product should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating this product.

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