Perneczky Aneurysm Clip 2 Applying Forceps Instructions for Use

Locking mechanism Contraindications The Perneczky Aneurysm Clip 2 Applying Forceps may only be used in combination with the corresponding Perneczky Aneurysm Clips 2 and are contraindicated for all other applications. Using the clip applying forceps for other manufacturers‘ aneurysm clips is not permitted.

EN

IFU Perneczky Aneurysm Clip 2 Applying Forceps

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Instructions for Use Important instructions for use! Please read this information before using the instrument! By purchasing these instruments, you have chosen very high quality products made in Germany. To ensure the function and safety of the instrument long term please observe the following points: First use of new instruments All instruments of adeor medical AG are delivered in non-sterile condition and must be cleaned and sterilized before use. Therefore, please pay attention to the following instructions (see chapter “Preparation (cleaning, disinfection and sterilization)“). Exempted from that are all instruments marked as “sterile“. Safety control Before each use, it is important to visually inspect the Clip- Applying Forceps. Make sure that there are no cracks, breaks or me-chanical malfunctions. Pay attention on critical points such as tips, cuttings, lockings and on all movable parts. Usage/Application The Perneczky Aneurysm Clip 2 Applying Forceps serve for opening and closing the Perneczky Aneurysm Clips 2. Using the forceps, the Aneurysm Clip is applied, repositioned or removed in the target tissue. The Clip-Applying Forceps have no function of their own and may only be used in combination with the suited Perneczky Aneurysm Clips 2.

Handling Treat these surgical instruments always with the necessary care. Take measures for protection against damages in transporting, cleaning, maintenance, sterilization and storage. Avoid contact of the instruments with ab-rasive substances (see chapter “Resilience of the material“); as this can lead to corrosion and impairment of the function up to complete unusability. This particularly applies for the use of acids or abrasive cleaners (it is vital to read and observe the directions of the cleaning agent producer!). The Clip-Applying forceps with marking MINI or STANDARD must only be operated with the respective MINI or STANDARD Aneurysm clips.

HANDLES

CLIP

Jaws fully closed ––> no clip

In the case of a snapped locking mechanism the clip is fixed in the applying forceps and partially opened. (The opening of the clip in fixed position can vary from one clip applying forceps to another

Memory Shaft DESCRIPTION

The handles of the clip applying forceps are fully straddled. The locking mechanism is not locked.

Put the clip into the slots of the jaws and press the handles of the applying forceps carefully until the mechanism locks. Please note: The function of the locking mechanism should be controlled before the insertion of the clip!

Note for Perneczky Aneurysm Clip 2 Memory Applying Forceps The special shape of Perneczky Aneurysm Clip 2 Memory Applying Forceps offers the user the best possible view over the surgery field. The memory shaft allows bending of the shaft and the jaws in almost every direction and position. After sterilization the memory shaft turns back into its original bayonet condition. The locking mechanism has been integrated in the handle of the Clip-Applying forceps to protect it from external forces. Special attention must be paid to the fact that this ClipApplying forceps has to be cleaned and sterilized separately in appropriate containers in order to protect the function of this locking device.

Full spread/ opening of the clip

Compress the handles of the applying forceps completely. The locking mechanism is untied automatically. lmportant: Both handles have to be pressed through completely to untie the locking mechanism

The memory shaft should be held with both hands in the area where the bending is required. Attention: Do not bend the memory shaft in the connection areas of the shaft. lncreased risk of breaking! After sterilization the memory shaft turns back into its original bayonet condition.

Preparation (cleaning, disinfection and sterilization) of Perneczky Aneurysm Clip 2 Appliers General basics All instruments are delivered in non-sterile condition and must be cleaned, disinfected and sterilized before use (cleaning and disinfection after removing the transport protection packing (including jaw protection) and sterillzation after packaging). Effective cleaning and disinfection is an essential requirement for effective sterilization. As you are responsible for the sterility of the Instruments during use, please see to it – that only sufficiently device- and productspecifically validated procedures are used for the cleaning/disinfection and sterilization. – that the used devices (disinfector, sterilizer) are maintained and checked on a regular basis and – that the validated parameters are complied with in every cycle. Please ensure already during the use to collectcontaminated instruments separately and do notput them back into the instruments tray in order to avoid stronger contamination of the equippedinstruments tray. Clean/disinfect the contaminated instruments, subsequently sort them back into the instruments tray and then sterilize the completely equipped instruments tray. Please also comply with the legal regulations applicable in your country and the doctor‘s office‘s/ hospital‘s sanitation regulations. This applies inparticular to the different specifications regarding effective prion inactivation.

The jaw protection serves only for protection during transport and sterilization; cleaning/disinfection with the jaw protection on is not permissible in any case. Cleaning and disinfection Basics lf possible, a machine procedure (disinfector) should be used for cleaning and disinfection. Due to the significantly lower effectiveness and reproducibility, a manual procedure – even when an ultrasound bath is employed – may only be used if no machine procedure is available. The pre-treatment must be performed in both cases. Pre-treatment Major contaminations must be removed from the clip-applying forceps immediately after use (within a maximum of 2 hours). Remove the jaw protection, unlatch the grip spring, if required, and bring the forceps into an opened position. Use running water or a disinfectant solution for that; the disinfectant should be aldehyde-free (otherwise, blood contaminations would be preserved) and have proven efficacy (e.g. VAH/ DGHM or FDA authorization or CE labeling), be suited for the disinfection of the clip-applying forceps and be compatible with the clip-applying forceps (see section “Resilience of the material“). Only use a soft brush or a clean soft cloth that you use only for this purpose, never metal brushes or steel wool, for manually removing contaminations. lf applicable: Dismantle the forceps as far as possible and remove the jaw protection. Rinse all lumina of the clip-applying forceps five times using a disposable syringe (minimum volume 10 ml). Move the mobile parts forth and back several times during the precleaning. Please bear in mind that the disinfectant used during the pre-treatment is only for protection of persons and cannot act as a substitute for the disinfection step performed later (after the cleaning).

Cleaning/disinfection using a device (disinfector/cleaning and disinfection device) When selecting the disinlector, it must be ensured – that the disinfector always has proven efficacy (e.g. DGHM or FDA authorization or CE labeling according to DIN EN ISO 15883), – that – if possible – a tested program for thermal disinfection (A0- value > 3000 or – for older devices – at least 5 min at 90° C) is used (if chemical disinfection is used, there is the risk of residues of the disinfectant on the aneurysm clip-applying forceps), – that the used program is suited for applying forceps and contains sufficient rin sing cycles, – that only sterile or low-germ (NMT 10 germs/ ml) and low- endotoxin (NMT 0.25 endotoxin units/ml) water (e.g. purilied water/ highly purified water) is used, – that the air used for drying is filtered and – that the disinfector is maintained and checked on a regular basis. When selecting the cleaning agent system used, it must be ensured – that it is generally suited lor cleaning aneurysm clip-applying forceps from metals and plastics, – that – unless thermal disinfection is used – a suited disinfectant with proven efficacy (e.g. DGHM or FDA authorization or CE labeling) is additionally used and that it is compatible with the cleaning agent used and – that the chemieals used are compatible with the applying forceps (see section “Resilience of the material“). The concentrations specified by the manufacturer of the cleaning agent/disinfectant must in any case be complied with. Procedure: 1. Put the dismantled applying forceps into the disinfector. Please ensure that the forceps do not touch each other. Place the forceps in opened position (it may be requi red to unlatch the grip-spring for this). lf applicable: Connect all lumina of the applying forceps to the rinsing connector of the disinfector. 2. Start the program. 3.Take the applying forceps out of the disinfector after the program is finished. 4. Check and package the applying forceps as

quickly as possible after taking them out (see the sections “Checking“ and “Packaging“), if appropriate after additionally drying at a clean place. The general suitability of the applying forceps for effective cleaning and disinfection using a machine was confirmed by an independent certified test laboratory using the disinfector G 7836 CD (thermal disinfection, Miele & Cie. GmbH & Co., Gütersloh) and the cleaning agent Neodisher mediclean (Dr. Weigert GmbH & Co. KG, Hamburg). The procedure described above was taken into account in doing so. Manual cleaning and disinfection When selecting the cleaning agent and disinfectant used, it must be ensured – that they are generally suited for cleaning/disinfecting instruments from metals and plastics, – that the cleaning agent – if applicable – is suited for ultrasound cleaning (no formation of foam), – that a disinfectant with proven efficacy (e.g. VAH/ DGHM or FDA authorization or CE labeling) is used and that it is compatible with the cleaning agent used and that the chemicals used are compatible with the instruments (see section “Resilience of the material“). Combined cleaning agents/disinfectants should not be used, if possible. Combined cleaning agents/ disinfectants can only be used in cases of very slight contamination (no visible contaminations). The concentrations and contact times specified by the manufacturer of the cleaning agent/disinfectant must in any case be complied with. Use only freshly-made solutions, only sterile or low-germ (NMT 10 germs/ml) and low-endotoxin (NMT 0.25 endotoxin units/ml) water (e.g. purified water/highly purified water) and only filtered air for drying. Procedure: Cleaning 1. Dismantle the applying forceps as far possible. 2. Put the dismantled forceps into the cleaning bath for the specified contact time such that the forceps are sufficiently covered (use ultrasound support or a soft brush, if

appropriate). Please ensure that the instruments do not touch each other. If applicable: Rinse all lumina of the clip-applying forceps at least five times at the beginning and the end of the contact time using a disposable syringe (minimum volume 10 ml). Move all movable parts at least five times at the beginning and the end of the contact time back and forth. and the end of the contact time back and forth. 3. Take the forceps out of the cleaning bath then and thoroughly rinse them off for at least 1 min under running water. II applicable: Rinse all lumina of the clipapplying forceps five times using a disposable syringe (minimum volume 10 ml). 4. Check all applying forceps (see section “Checking“ and “Maintenance“). Disinfecion 5. Put the dismantled, cleaned and checked clip-applying forceps into the disinfection bath for the specified contact time such that the forceps are sufficiently covered. Please ensure that the forceps do not touch each other. If applicable: Rinse all lumina of the clip-applying forceps at least five times at the beginning and the end of the contact time using a disposable syringe (minimum volume 10 ml). Move all movable parts at least five times at the beginning and the end of the contact time back and forth. 6. If applicable: Rinse all lumina of the clipapplying forceps five times using a disposable syringe (minimum volume 10 ml). 7. Dry the clip-applying forceps by blowing filtered compressed air. 8. Package the clip-applying force ps as quickly as possible after taking them out (see section “Packaging“, if required, after letting them dry in a clean place). The general suitability of the applying forceps for effective manual cleaning and disinfection was confirmed by an independent certified test laboratory using the cleaning agent Cidezyme/ Enzol and the disinfectant Cidex opa (Johnson & Johnson GmbH, Norderstedt). The procedure described above was taken into account.

Checking Check all applying forceps after cleaning or cleaning/ disinfection for corrosion, damaged surfaces, splitting and contaminations and scrap damaged aneurysm clip-applying forceps (please refer to the section “Reusability“ for re-use limitation in numbers). Applying forceps that are still contaminated must be cleaned and disinfected again. Maintenance – Note for applying forceps with joints (especially Perneczky Aneurysm Clip 2 Memory applying forceps) – Treat the joints of the Memory applying forceps with instrument oil after every preparation. It should be ensured that only instrument oils (white oil) that – taking into account the maximum sterilization temperature used – are authorized for vapor sterilization and have proven biocompatibility are used and that the jaw and joint parts are only treated with as little oil as possible. – Scrap outworn, corroded, deformed, porous or otherwise damaged clip-applying forceps. – Instruments which are sent in for repair works must be prepared completely for sanitary reasons.

Packaging Sort the cleaned and disinfected clip-applying forceps into the corresponding sterilization tray. Please package the applying forceps or trays in disposable sterilization packs (single or double pack) and/or sterilization containers that comply with the following requirements: – DIN EN ISO/ANSI AAMIISO 11607 – suited for vapor sterilization (temperature resistance up to NLT 141°C (286° F), sufficient vapor permeability) – sufficient protedion of the aneurysm clips/ sterilization packs

against mechanical damage – regular maintenance in accordance with the manufacturer‘s specifications (sterilization container)

Storage Do not store the applying forceps in metal containers, except for stainless steel or aluminum containers. Avoid direct exposure to sunlight.

Sterilization Only the sterilization procedures listed in the following shall be used for sterilization; other sterilization procedures are impermissible.

After the sterilization, the instruments must be stored dry and free from dust in the sterilization pack.

Vapor sterilization – fractionated vacuum procedure1 (with sufficient drying of the product) – Vapor sterilizer in compliance with DIN EN 13060/ DIN EN 285 Validated according to DIN EN ISO 17665 (previously: DIN EN 554/ ANSI AAMI ISO 11134) (valid IQ/OQ (consignment) and product-specific performance qualification) Maximum sterilization temperature 138° C (280° F; plus tolerance according to DIN EN ISO 17665 (previously: DIN EN 554/ ANSI AAMIISO 11134)) – Sterilization time (exposure time at sterilization temperature) NLT 20 min at 121° C (250° F) or NLT 3 min2 at 132° C (270° F)/ 134 ° C (273° F) 1 The use of the less elledive gravitation proce- dure is only permitted if the fractionated vacuum procedure is not available; it may require significantly longer exposure times and must be confirmed with a product-, procedure and device-specific validation under the user‘s sole responsibility. 2 or 18 min (prion inactivation) The general suitability of the applying forceps for effective vapor sterilization was confirmed by an independent certified test laboratory using the vapor sterilizer Systec V-150 (Systec GmbH Labor- Systemtechnik, Wettenberg) and the fractionated vacuum procedure. Typical conditions in hospitals and doctor‘s offices as well as the procedure described above were taken into account in doing so. Flash sterilization is never permissible. Do not use hot air sterilization, radio-sterilization, formaldehyde or ethylene oxide sterilization and plasma sterilization, either.

Resilience of the material When selecting the cleaning agents and disinfectants, please ensure that they do not contain the following components: – organic, mineral and oxidizing acids (minimum permissible pH value 5.5) –strong Iye (maximum permissible pH value 10.9, neutral/enzymatic or slightly alkaline cleaning agent recommended) –organic solvents (e.g. alcohols, ether, ketones, benzines) – oxidants (e.g. hydrogen peroxides) – halogens (chlorine, iodine, bromine) – aromatic/halogenated hydrocarbons Never clean any aneurysm clip applier and tray with metal brushes or steel wool. All clip appliers and trays may only be exposed to temperatures NMT 141° C (286° F)! Reusability The clips-applying forceps can – if appropriate care is taken and they are undamaged and not contaminated – be reused up to 500 times; the user himself/herself shall be responsible if he/ she uses the forceps more often or uses damaged or contaminated forceps. Any liability shall be excluded in case of noncompliance. Caution: Federal law restricts this device to sale by or on order of a physician!

Explanations of used symbols Consult operating instructions Catalogue number Manufacturer not Sterile Lot Number CE-sign

adeor medical AG Martinshof 5 83626 Valley, Germany +49 (0) 89 / 74 44 23 98 www.adeor.com Version: 2021-03-DE_EN