rime Series Stretcher Model 1115XXX Big Wheel Operations Manual Rev AD.0

Symbols Refer to instruction manual/booklet Consult instructions for use General warning Caution Warning; crushing of hands

Warning; non-ionizing radiation

No pushing

Do not store the oxygen bottle

Do not lubricate

Telecommunications and Digital Government Regulatory Authority logo for United Arab Emirates

Australia/New Zealand Regulatory Compliance Mark (RCM)

New Zealand radio compliance mark

US (FCC) wireless conformity mark

CE mark Authorized representative in the European Community

European medical device

Importer

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UK Conformity Assessment mark

Unique device identifier

CH REP

Authorized representative in Switzerland Catalogue number Lot (batch) code

 

Serial number For US Patents see www.stryker.com/patents Manufacturer

Date of manufacture

Safe working load

Maximum patient weight Mass of equipment with safe working load Direct current

~

Alternating current

Dangerous voltage

Protective earth ground IPX6

Protection from powerful water jets Type B applied part

87VL

EN

P r i m e and P r i m e X : Medical Equipment Classified by Underwriters Laboratories Inc. With Respect to Electric Shock, Fire, and Mechanical Hazards Only in Accordance with ANSI/AAMI ES60601-1: 2005 and A1:2012, CAN/CSA-C22.2 No. 60601-1:14. For P r i m e X option, Associated Equipment of X-ray Equipment IEC 60601-2-54. P r i m e C o n n e c t : Medical Equipment Classified by Underwriters Laboratories Inc. With Respect to Electric Shock, Fire, and Mechanical Hazards Only in Accordance with ANSI/AAMI ES606011:2005, A1:2012, and A2:2021, CAN/CSA-C22.2 No. 60601-1:14 and A2:2022 (R2022).

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In accordance with European Directive 2012/19/EU on Waste Electrical and Electronic Equipment (WEEE) as amended, this symbol indicates that the product should be collected separately for recycling. Do not dispose of as unsorted municipal waste. Contact local distributor for disposal information. Ensure infected equipment is decontaminated prior to recycling. Lubricate

Lift here This way up

Keep dry

Fragile, handle with care

Stacking limit by number

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Table of Contents Warning/Caution/Note Definition ...3 Summary of safety precautions ...3 Pinch points ...6

Introduction ...7 Product description ...7 Intended use ...7 Indications for use...7 Intended users...8 Clinical benefits ...8 Contraindications ...8 Expected service life ...8 Disposal/recycle ...8 Specifications ...8 Wi-Fi radio specifications, Prime Connect...10 Product illustration, Prime and Prime Connect...12 Product illustration, Prime X...13 Applied parts, electric litter ...14 Applied parts, Prime X...15 Contact information ...15 Serial number location...16

Setup ...17 Setting up bed exit over wired nurse call, Prime Connect ...17 Setting up iBed Locator, Prime Connect...18

Operation ...19 Product features ...19 Applying and releasing the brakes...19 Base controls...20 Raising the product ...20 Lowering the product...21 Positioning the product in Trendelenburg ...21 Positioning the product in reverse Trendelenburg ...21 Transporting a patient ...22 Transporting a patient without Big Wheel ...22 Transporting a patient with Big Wheel...23 Positioning or stowing the head end push handles...24 Raising the siderail...25 Lowering the siderail ...25 Positioning the product with the siderail patient control panel, electric litter ...26 Operator control panel, electric litter ...26 Locking and unlocking the patient control panel lockout, electric litter ...27 Raising or lowering the Fowler backrest, non-electric litter...28 Raising or lowering the Fowler backrest, electric litter ...28 Raising or lowering the Gatch, non-electric litter ...29 Raising or lowering the Gatch, electric litter ...29 Positioning the recovery chair ...30 Storing objects in the base hood...31 Hanging devices with the pump rack option...31 Extending or retracting the power cord with the retractable cord reel ...32 Scale system and bed exit ...32 Operator keypad icon/button identification ...33 Weighing a patient, Prime and Prime X ...34 Weighing a patient, Prime Connect ...35 Locking the scale unit of measure, Prime and Prime X ...35 Arming or disarming bed exit, Prime...36 Arming or disarming bed exit, Prime Connect ...36 1115-309-001 Rev AD.0

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Changing the bed exit alarm pattern, Prime ...37 Changing the bed exit alarm pattern, Prime Connect ...37 Changing the bed exit alarm volume, Prime...37 Changing the bed exit alarm volume, Prime Connect ...38 Charging the battery pack ...38 Replacing the batteries for the scale system, non-electric litter ...39 Accessories and parts ...39 Attaching the defibrillator tray ...42 Converting the defibrillator tray/foot extender to a defibrillator tray ...43 Converting the defibrillator tray/foot extender to a foot extender ...43 Attaching the footboard/chart holder ...44 Attaching the IV caddy ...44 Positioning or stowing the foot supports, Prime ...45 Positioning the two-stage permanently attached IV pole ...46 Positioning the three-stage permanently attached IV pole...47 Attaching and positioning the removable IV pole ...48 Attaching the upright oxygen bottle holder ...49 Extending or stowing the serving tray holder/footboard...49 Attaching the siderail pads ...50 Locating the patient restraint strap tie-ins ...50 Positioning the upright X-ray cassette holder, Prime X...50 Positioning the lateral X-ray cassette holder, Prime X...51 Inserting or removing X-ray cassettes, Prime X...52

Cleaning and disinfecting with SideKick ...54 Cleaning ...55 Cleaning the product ...55 Cleaning the product using a cart washer...55 Cleaning the mattress ...56 Remove iodine ...57 Special instructions ...57

Disinfecting ...58 Disinfecting the product ...58 Disinfecting the mattress ...58

Preventive maintenance ...60 Wireless notifications ...62 Wireless coexistence notifications ...62

EMC information ...63

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Warning/Caution/Note Definition The words W A R N I N G , C A U T I O N , and N O T E carry special meanings and should be carefully reviewed. WARNING Alerts the reader about a situation which, if not avoided, could result in death or serious injury. It may also describe potential serious adverse reactions and safety hazards. CAUTION Alerts the reader of a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to the user or patient or damage to the product or other property. This includes special care necessary for the safe and effective use of the device and the care necessary to avoid damage to a device that may occur as a result of use or misuse. N o t e - Provides special information to make maintenance easier or important instructions clearer.

Summary of safety precautions Always read and strictly follow the warnings and cautions listed on this page. Service only by qualified personnel. WARNING • Always allow the product to reach room temperature before you set up the product or test functional operations. Permanent product damage may occur. • Always operate the product when all operators are clear of the mechanisms. • Always use care when you handle the power cord. Entanglement, damage to the power cord, or potential shock hazards may occur. If the power cord is damaged, remove the product from service and contact the appropriate maintenance personnel. • Always plug the product into a grounded, hospital grade wall outlet. You can only achieve grounding reliability when you use a hospital grade wall outlet. This product is equipped with a hospital grade plug to protect against electric shock hazard. • Always apply the brakes when a patient is getting on the product or off the product or when the product is not moving. Injury could result if the product moves while a patient is getting on the product or off the product. • Always position the patient in the center of the product. • Always lock the siderails in the highest height position and lower the product to the lowest height position when you leave a patient unattended. • Always remove any devices that may be in the way before you raise or lower the litter. • Do not sit on the end of the product. The product may tip. • Always lock the siderails in the highest height position with the sleep surface horizontal and lower the product to the lowest height position when you transport a patient. • Do not transport the product laterally on inclines greater than 5.7 degrees (10% grade) to avoid product tipping. • Always use extra caution when you use a mattress thicker than 2.5 in. or a mattress overlay with P r i m e X . • Always keep the patient’s limbs away from the siderail spindles when you raise or lower the siderail. • Do not allow the siderails to lower on their own. • Always keep hands and fingers clear of the Fowler backrest release handles and the Fowler backrest frame when you lower the Fowler backrest. • Always use caution when you raise and lower the Fowler backrest while a patient is on the product. Use proper lifting techniques and get help, if necessary. • Always keep hands and fingers clear of the foot end push handles when you lower the Gatch. • Always keep device lines on the pump rack away from the Gatch handles. • Always make sure that devices on the pump rack can pass through door openings. • Do not lift the product by the pump rack. • Always unplug the power cord from the wall outlet before you transport or clean the product. • Always use the retractable cord reel to store the power cord inside the base when you transport the product.

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• Do not use the scale system, electric lift, or electric litter options adjacent to or stacked with other devices. If adjacent or stacked use is necessary, the scale system, electric lift, or electric litter options should be observed to make sure that all devices operate in the configuration in which they will be used. • Do not place items that weigh more than 30 lb (14 kg) on the defibrillator tray. Always strap down all devices that you place on the defibrillator tray. • Always use caution if the defibrillator tray/foot extender, footboard/chart holder, or upright oxygen bottle holder is attached to avoid pinching your fingers when you position the foot end push handle option. • Do not place items that weigh more than 30 lb (14 kg) on the defibrillator tray/foot extender. Always strap down all devices that you place on the defibrillator tray. • Always secure the IV pole to the IV caddy when you transport the product. • Always store the IV caddy when not in use to avoid product damage. • Do not sit on the foot supports. This may cause the product to tip. • Always clear your fingers from the mechanisms when you operate the foot supports. • Always stow the foot supports when you transport a patient with the product. • Always tighten the foot supports before you use the foot supports. • Do not operate the scale system with the foot supports. Inaccurate readings may occur. • Do not operate bed exit with the foot supports. Inaccurate readings may occur. • Do not use the IV pole as a push/pull device. Product damage may occur. • Do not place objects that exceed 40 lb (18 kg) in the upright oxygen bottle holder. • Do not place objects that exceed 30 lb (14 kg) on the serving tray. • Always use caution when you attach restraint straps. Patient or operator injury may occur. Physical restraints, even if secured, may result in serious harm to patients and operators, including entanglement, entrapment, physical injury, or death. • Always attach restraint straps or devices only at the identified attachment points of the product. Failure to do so may result in patient or operator injury. Do not attach restraint straps to the siderail. • Always refer to the applicable state and federal restrictions and regulations and the appropriate facility protocols before you use any restraint strap or device. • Always take protective measures when you use the upright or lateral X-ray cassette holder. The X-ray cassette holder does not protect against radiation. • Always refer to local, state, and federal guidelines in addition to facility protocols for safety before you use P r i m e X with radiation generating devices. Radiation generating devices may produce residual, stray, or scattered radiation. • Always follow the Positioning the upright X-ray cassette holder - Prime X option instructions to insert the X-ray cassette. • Always use caution when you take X-rays with the Fowler backrest in the upright position or when you use a lateral cassette. • Always follow the Positioning the lateral X-ray cassette holder - Prime X option instructions to insert the X-ray cassette. • Do not clean, service, or perform maintenance while the product is in use. • Do not immerse the mattress in cleaning or disinfectant solutions. Excess moisture could cause product malfunction that results in product damage or patient injury. • Do not allow fluid to pool on the mattress. Fluids can cause corrosion of components and may cause the safety and performance of this product to become unpredictable. • Always inspect mattress covers for tears, punctures, excessive wear, and misaligned zippers every time you clean the covers. Remove and replace a damaged mattress to prevent cross-contamination. • Do not steam clean, pressure wash, hose off, or ultrasonically clean mattresses. These methods of cleaning may void the product’s warranty. • Do not steam clean, hose off, or ultrasonically clean the product. Use of these methods of cleaning is not recommended and may void the product’s warranty. • Always disinfect the mattress between patients. Failure to do so could result in cross-contamination and infection. • Portable RF communications equipment, including peripherals such as antenna cables and external antennas, should be no closer than 12 inches (30 cm) to any part of the P r i m e S e r i e s stretcher, including cables specified by the manufacturer. • Avoid stacking or placing equipment adjacent with other equipment to prevent improper operation of the product. If such use is necessary, carefully observe stacked or adjacent equipment to make sure that they operate properly. • The use of accessories, transducers, and cables, other than those specified or provided by the manufacturer, could result in increased electromagnetic emissions or decreased electromagnetic immunity and result in improper operation.

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CAUTION • Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in this manual. • Do not modify the product or any components of the product. Modifying the product can cause unpredictable operation resulting in injury to patient or operator. Modifying the product also voids its warranty. • Do not use the hydraulics on the base to raise the product with a patient lift under the product. • Do not apply the steer pedal when B i g W h e e l is resting on a threshold or other raised area. The force required to apply B i g W h e e l will be higher than normal and may cause product damage. • Do not exceed the 200 lb (90.7 kg) weight capacity of the Gatch. • Always make sure that the Gatch prop rod is secure before you raise or lower the Gatch. • Do not sit or stand on the Gatch. • Always use caution when you attempt to lower the Gatch while the product is unpowered. Gravity may cause a rapid drop of the Gatch. • Do not place objects that exceed 60 lb (27 kg) in the base hood. • Do not sit, step, or stand on the base hood. • Do not exceed the 40 lb (18 kg) weight capacity of the pump rack. • Do not use the pump rack as a push/pull device. Product damage may occur. • Do not use the scale for patients under 50 lb (22.7 kg). • Do not use the scale system reading as a reference for medical treatment. • Always raise the IV pole before you attach the defibrillator tray/foot extender to the product. If you do not raise the IV pole, the foot extender will not operate. • Do not use the IV pole as a push/pull device. Product damage may occur. • Do not hang IV bags that exceed 40 lb (18 kg) on the IV pole. • Always make sure that the IV pole is at a low height to pass through door openings when you transport a patient. • Do not use abrasive cleaners to clean the display enclosure for the scale system option. Do not allow cleaning solutions or other fluids to pool on the display unit. Dry all surfaces after spills or cleaning.

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Pinch points

Figure 1 – Prime X

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Introduction This manual assists you with the operation or maintenance of your Stryker product. Read this manual before operating or maintaining this product. Set methods and procedures to educate and train your staff on the safe operation or maintenance of this product. CAUTION • Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in this manual. • Do not modify the product or any components of the product. Modifying the product can cause unpredictable operation resulting in injury to patient or operator. Modifying the product also voids its warranty. Note • This manual is a permanent part of the product and should remain with the product even if the product is sold. • Stryker continually seeks advancements in product design and quality. This manual contains the most current product information available at the time of printing. There may be minor discrepancies between your product and this manual. If you have any questions, contact Stryker Customer Service or Technical Support at 1-800-327-0770.

Product description The Stryker P r i m e S e r i e s stretcher is a wheeled device which consists of a platform mounted on a wheeled frame that is designed to support patients in a horizontal position. A stretcher provides the operator with a method of transporting patients within the interior of a healthcare facility by health professionals or trained representatives of the facility. The device has siderails and has the option available to support the temporary or permanent placement of IV poles, along with various other options and accessories to assist with the transport of the patient. The Stryker Model 1115 P r i m e S e r i e s stretcher with B i g W h e e l decreases start-up force and steering effort to reduce physical strain. The Stryker P r i m e S e r i e s stretcher with bed exit aids in patient safety by detecting when the patient’s center of gravity moves beyond the healthcare provider’s selected zone and activating an audible and visible alarm at bedside. The Stryker P r i m e C o n n e c t stretcher provides an additional alarm at the nurse station through nurse call. Alarm signal transmission can be wired or for P r i m e C o n n e c t stretchers, equipped with both a wireless module and connected to the i B e d Locator, sent wirelessly to a remote dashboard. The Stryker P r i m e C o n n e c t stretcher equipped with a wireless module can facilitate wireless communication of multiple stretcher data parameters, such as bed exit on and off status, patient weight when equipped with a scale, and location. Each stretcher is associated with a particular room or bay location enabled by an i B e d Locator; a battery powered module that mounts to the hospital wall in a fixed location and communicates to applicable stretchers using Infrared (IR) lightemitting diode (LED) technology as a required component for overall wireless connectivity. The stretcher data parameters can be integrated with various systems within the healthcare facility, such as the healthcare facility’s electronic health record (EHR) system, nurse call, and mobile communication devices.

Intended use The P r i m e S e r i e s stretcher provides a method of transporting patients within a healthcare facility by healthcare professionals or trained personnel.

Indications for use The P r i m e S e r i e s stretcher with B i g W h e e l has two big wheels to reduce the startup force required to move the stretcher. The P r i m e S e r i e s stretcher may be used as a short-term outpatient clinical evaluation, treatment, minor procedure, and short-term outpatient recovery platform. The stretcher may include use in, but is not limited to: •

Emergency department (ED)

•

Trauma area

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•

Post-anesthesia care unit (PACU)

The P r i m e S e r i e s stretcher may be used for minor procedures and short-term stay (treatment and recovery). The P r i m e S e r i e s stretcher is not for use for long-term inpatient treatment and recovery. The P r i m e S e r i e s stretcher has a safe working load up to 700 lb (318 kg) and is intended to be used with all patients, including those mildly to critically ill. The stretcher may also be used to transport deceased patients within an enclosed healthcare facility. The P r i m e X option provides an articulating radiographic patient support surface and a platform below the patient support surface for X-ray cassette placement. P r i m e X option is intended to allow the capture of clinical X-rays (AP full body, optional full body lateral, and optional upright chest) when used with a medical X-ray system.

Intended users Intended operators of this product are healthcare professionals (nurses, nurses aids, doctors) and transporters.

Clinical benefits Patient transport, facilitate treatment, and diagnostic

Contraindications None known

Expected service life The P r i m e S e r i e s stretchers have a 10 year expected life under normal use conditions and with appropriate periodic maintenance.

Disposal/recycle Always follow the current local recommendations and/or regulations governing environmental protection and the risks associated with recycling or disposing of the equipment at the end of its useful life.

Specifications 26 in. width

30 in. width

Prime manual only

30 in. width

Prime X only

700 lb

318 kg

700 lb

318 kg

700 lb

318 kg

675 lb

306 kg

675 lb

306 kg

675 lb

306 kg

N o t e - Safe working load indicates the sum of the patient, mattress, and accessory weight.

Maximum patient weight

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26 in. width

30 in. width

Prime manual only

30 in. width

Prime X only

Overall length

85 in. (± .5 in.)

215.9 cm

85 in. (± .5 in.)

215.9 cm

85 in. (± .5 in.)

215.9 cm

Overall length (litter extension option)

89.9 in. (± .75 in.)

228.3 cm

89.9 in. (± .75 in.)

228.3 cm

NA

NA

Overall width (siderails up)

34 in. (± 1 in.)

86.4 cm

38 in. (± 1 in.)

96.5 cm

38 in. (± 1 in.)

96.5 cm

Overall width (siderails down)

26 in. (± .5 in.)

66 cm

30.5 in. (± .5 in.)

77.5 cm

30.5 in. (± .5 in.)

77.5 cm

Minimum height

20.75 in. (± 1 in.)

52.7 cm

20.75 in. (± 1 in.)

52.7 cm

23.25 in.

59.1 cm

Maximum height

34 in. (± 1 in.)

86.4 cm

34 in. (± 1 in.)

86.4 cm

36.5 in. (± 1 in.)

92.7 cm

Maximum cassette dimension

Side

Not applicable

19.87 in.

50.5 cm

Head end

Not applicable

21 in.

53.3 cm

Fowler backrest angle

0° to 90° (± 5°)

Gatch height

5.5 in. (14 cm) minimum

Trendelenburg/reverse Trendelelburg

± 17° (± 3°) 2.5 in. nominal

Minimum clearance

Not applicable

6.4 cm

2.5 in. nominal

6.4 cm

2.5 in. nominal

6.4 cm

1.75 in. under the hydraulic jacks

4.5 cm

1.75 in. under the hydraulic jacks

4.5 cm

1.75 in. under the hydraulic jacks

4.5 cm

1 in. under Big Wheel

2.5 cm

1 in. under Big Wheel

2.5 cm

1 in. under Big Wheel

2.5 cm

Attenuation equivalent (aluminum equivalence)

Not applicable

Scale system weight operating range

50 lb (22.7 kg) to 700 lb (318 kg)

Scale system accuracy

± 3 lb (1.3 kg) for weights less than 100 lb (45 kg) and ±3% for weights greater than or equal to 100 lb (45 kg)*

Maximum value allowed is 1.7 mm Al

*To meet the scale system accuracy claim, the patient surface must be in the flat position (Fowler backrest and Gatch down) and the product cannot exceed 5 degrees of Trendelenburg/reverse Trendelenburg. Electric

Electric litter

Electric lift

120 VAC, 60Hz, 10A

120 VAC, 60Hz, 10A

240 VAC, 50/60 Hz, 5A

240 VAC, 50/60 Hz, 5A

Continuous operation with intermittent loading is 1 min. ON/20 min. OFF

Continuous operation with intermittent loading is 1 min. ON/20 min. OFF

Electrical requirements

Duty cycle

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Scale system

Non-electric litter

Electric lift

Battery type

4 x AA battery (4 X 1.5 VDC) alkaline type (LR6)

4 x AA battery (4 X 1.5 VDC) alkaline type (LR6)

Battery voltage

6.0 VDC

6.0 VDC

Scale system

Electric litter

Electric lift

Battery type

1 x rechargeable lithium ion battery pack (0058-135-000)

Not applicable

Battery voltage

10.8 VDC, 2.4Ah

Not applicable

Scale system with bed exit

Electric litter

Electric lift

Battery type

1 x rechargeable lithium ion battery pack (0058-134-000)

Not applicable

Battery voltage

10.8 VDC, 4.8Ah

Not applicable

Stryker reserves the right to change specifications without notice. N o t e - This product is not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide. Environmental conditions

Storage and transportation

Operation Prime and P r i m e X

Prime Connect

100 °F (38 °C)

Temperature

95 °F (35 °C)

50 °F (10 °C)

50 °F (10 °C)

140 °F (60 °C) -4 °F (-20 °C) 95%

75%

Relative humidity 10%

30% 1060 hPa

1060 hPa

Atmospheric pressure 700 hPa

500 hPa

N o t e - The scale system/bed exit operation temperature range is 61 °F (16 °C) to 79 °F (26 °C). Specifications listed are approximate and may vary from product to product or by power supply fluctuations. For product feature availability for your model, see Product features (page 19).

Wi-Fi radio specifications, Prime Connect For P r i m e C o n n e c t models with Wi-Fi enabled wireless communication. For product feature availability for your model, see Product features (page 19). Hereby, Stryker Medical declares that the radio equipment type wireless LAN device is in compliance with Directive 2014/ 53/EU. The full text of the EU declaration of conformity is available at the following internet address: techweb.stryker.com/Stretcher/index.html. Note • P r i m e C o n n e c t security white paper available upon request. • P r i m e C o n n e c t MDS2 form available upon request.

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• P r i m e C o n n e c t software bill of materials available upon request. Customer WLAN environment Microwave ovens

Avoid using microwave ovens near Stryker wireless products as this will cause degradation of service or no service due to electromagnetic or radiofrequency (RF) interference. See Wireless coexistence notifications (page 62).

LTE-LAA cellular band

LTE-LAA introduces a new cellular band (B46) that coexist with 5GHz Wi-Fi (5150 MHz - 5925 MHz). Any cellular devices/repeaters should have this cellular band (B46) disabled to prevent degradation of service or no service due to electromagnetic or radio-frequency (RF) interference. See Wireless coexistence notifications (page 62).

Manufacturer/model

Silex SX-SDMAC-2832S+

Chipset

QCA9377-3

IEEE 802.11

a/b/g/n/ac

RF bands

2.4 GHz, 5 GHz AES and TKIP

Encryption N o t e - TKIP is not supported with WPA2. Authentication

WPA Personal/Enterprise and WPA2 Personal/Enterprise

802.1X

PEAP-MSCHAP v2

Client certificates

Cannot accept or upload certificates

Supported data rates

IEEE 802.11b: 1-11 Mbps IEEE 802.11a/g: 6-54 Mbps IEEE 802.11n: MCS 0-7 (1x1) IEEE 802.11ac: MCS 0-9 (1x1)

Hash function compatibility

SHA-1 and SHA-2 server-side certificate recognition for PEAP-MSCHAP v2 2.4 GHz: All channels supported 5 GHz: All channels supported

Channel plan

N o t e - Stryker recommends against the use of DFS and ISM channels. Leverage hospital SSID Supports fast roaming (802.11r and CCKM)

Other

Specification - Chipset QCA9377-3 Item

Unit Band 2.4GHz

Operating frequencies 5GHz

Frequency steps

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Mode

Min

Max

11b

2412

2472

MHz

11g/n/ac 20 MHz

2412

2472

MHz

11a/n/ac 20MHz

5180

5825

MHz

11n/ac 40MHz

5190

5795

MHz

2.4GHz

11b/g/n/ac 20MHz

5

MHz

5GHz

11a/n/ac 20MHz

20

MHz

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Specification - Chipset QCA9377-3 Item

Unit Band

Modulation types

Maximum ERP

Mode

Min

Max

11n/ac 40MHz

40

MHz

Not applicable

11b

DSSS (DBPSK, DQPSK, CCK)

Not applicable

Not applicable

11a/g/n

OFDM (BPSK, QPSK, 16QAM, 64QAM)

Not applicable

Not applicable

11ac

OFDM (BPSK, QPSK, 16QAM, 64QAM, 256QAM)

Not applicable

Not applicable

Not applicable

-8.648/21.352

dBW/dBm

Product illustration, Prime and Prime Connect

B

Q

A

C

C D

L M E F

D

P N O

E G

H

J D

I

K

Figure 2 – Prime and Prime Connect A

IV pole

J

Siderail latch

B

Head end push handle

K

Hydraulic release pedal

C

G l i d e a w a y siderail

L

Gatch release handle

D

Brake/steer pedal

M

B a c k S m a r t operator control panel

E

Pump pedal

N

Pump rack

F

Uni-lower pedal

O

Operator keypad

G

Big Wheel

P

Patient control panel lockout

H

Bumper, integrated

Q

B a c k S m a r t siderail patient control panel

I

Caster with integrated wheel cover

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For product feature availability for your model, see Product features (page 19).

Product illustration, Prime X

A E B B

C D E

K L

F G H

M

G F

I J

F

Figure 3 – Prime X A

Head end push handle

H

Uni-lower pedal

B

IV pole

I

Bumper, integrated

C

Cassette tray

J

Caster with integrated wheel cover

D

Patient surface with C l e a r v i e w T e c h n o l o g y deck

K

Siderail latch

E

G l i d e a w a y siderail

L

Pump rack

F

Brake/steer pedal

M

Operator keypad

G

Pump pedal

For product feature availability for your model, see Product features (page 19).

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Applied parts, electric litter

Figure 4 – Type B applied parts - electric litter For product feature availability for your model, see Product features (page 19).

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Applied parts, Prime X

Figure 5 – Type B applied parts - Prime X For product feature availability for your model, see Product features (page 19).

Contact information Contact Stryker Customer Service or Technical Support at: 1-800-327-0770. Stryker Medical 3800 E. Centre Avenue Portage, MI 49002 USA N o t e - The user and/or the patient should report any serious product-related incident to both the manufacturer and the Competent authority of the European Member State where the user and/or patient is established. To view your operations or maintenance manual online, see https://techweb.stryker.com/. Have the serial number (A) of your Stryker product available when calling Stryker Customer Service or Technical Support. Include the serial number in all written communication.

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Serial number location

A

Figure 6 – Serial number location

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