Aesculap M39101BG Ring Type Scissors and Spring
Technical Description
Ring-type scissors and spring-type scissors.
Note for U.S. users
This Instructions for Use is NOT intended for United States users. Please discard. The Instructions for Use for United States users can be obtained by visiting our website at www.aesculapusaifus.com. If you wish
to obtain a paper copy of the Instructions for Use, you may request one by contacting your local Aesculap representative or Aesculap’s customer service at 1-800-282-9000. A paper copy will be provided to you upon request at no additional cost.
About this document
Note
General risk factors associated with surgical procedures are not described in these instructions for use.
Scope
These instructions for use apply to ring-type and spring-type scissors in nearly all surgical disciplines.
Note
The applicable CE mark for the product can be seen on the label or packaging of the product. For article-specific instructions for use material compatibility and lifetime information, see B. Braun eIFU at eifu.bbraun.com
Safety messages
Safety messages make clear the dangers to patients, users, sr, and/or productsuct that could arise during the use of the product.
WARNING
Indicates a possible threat of danger. If not avoided, minor or moderate injury may result.
CAUTION
Indicates a possible threat of material damage. If not avoided, the product may be damaged.
- Clinical use
- Areas of use and limitations of use
- Intended use
Surgical scissors
The instruments are used to cut tissue and/or medical materials and supplies.
Dissecting scissors
The instruments are used to cut and/or dissect tissue.
Nail scissors
The instruments are used to cut or spfingernailsails and toenails and/or cuticles.
Bandage scissors and material scissors
The instruments are used to cut medical material supplies and/or clothing.
Micro scissors
The instruments are used to cut and/or dissect tissue during microsurgical procedures.
Indications
The instruments are used in a multitude of surgical procedures and interventions in almost all surgical disciplines, see Intended Use.
Contraindications
No contraindications for the product are currently known.
General safety information
To prevent damage caused by improper setup or operation, and to not compromise the mmanufacturer’swarranty and liability:
- Use the product only according to these instructions for use.
- Follow the safety and maintenance instructions.
- Ensure that the product and its accessories are operated and used only by persons with the requisite training, knowledge, and experience.
- Store any new or unused products in a dry, clean, and safe place.
- Before use, check that the product is in good working order.
- Keep the instructions for use accessible for the user.
Note
The user is obligated to report all severe events in connection with the product to the manufacturer and the responsible authorities of the state in which the user is located.
Notes on surgical procedures
It is the user’s responsibility to ensure that the surgical procedure is performed correctly. Appropriate clinical training as well as a theoretical and practical proficiency of all the required operating techniques, including the use of this product, are prerequisites for the successful use of this product. The user is required to obtain information from the manufacturer if there is an unclear preoperative situation regarding
the use of the product.
Sterility
The product is delivered in an unsterile condition.
- Clean the new product after removing its transport packaging and before its initial sterilization.
Application
Risk of injury and/or malfunction!
- Before each use, inspect the product for loose, bent, broken, cracked, worn, or fractured components.
- Always carry out a function test before each use of the product.
Validated reprocessing procedure
Note
Adhere to national statutory regulations, national and international standards and directives, and local, clinical hygiene instructions for sterile processing.
Note
For patients with Creutzfeldt-Jakob disease (CJD), suspected CJD, or possible variants of CJD, observe the relevant national regulations concerning the reprocessing of products.
Note
Mechanical reprocessing should be favored over manual cleaning as it gives better and more reliable results.
Note
Successful processing of this medical device can only be ensured if the processing method is first validated. The operator/ sterile processing technician is responsible for this.
Note
If there is no final sterilization, then a virucidal disinfectant must be used.
Note
For up-to-date information about reprocessing and material compatibility, see B. Braun eIFU at eifu.bbraun.com .The validated steam sterilization procedure was carried out in the Aesculap sterile container system.
General information
Dried or affixed surgical residues can make cleaning more difficult or ineffective and lead to corrosion. Therefore the time interval between application and processing should not exceed 6 h; also, neither fixating pre-cleaning temperatures >45 °C nor fixating disinfecting agents (active ingredient: aldehydes/alcohols) should be used.
Excessive measures of neutralizing agents or basic cleaners may result in a chemical attack and/or fading and the laser marking becoming unreadable visually or by machine for stainless steel. Residues containing chlorine or chlorides e.g. in surgical residues, medicines, saline solutions, and in the service water used for cleaning, disinfection,n, and sterilization will cause corrosion damage (pitting, stress corrosion)and destroy stainless steel products. These must be removed by rinsing thoroughly with demineralized water and then drying.
Additional drying, if necessary
Only process chemicals that have been tested and approved (e.g. VAH or FDA approval or CE mark) and which are compatible with the product’s materials according to the chemical manufacturer’s recommendations may be used for processing the product. All the chemical manufacturer’s application specifications must be strictly observed. Failure to do so can result in the following problems:
- Optical changes of materials, e.g. fading or discoloration of titanium or aluminum. For aluminum, the application/ process solution only needs to be of pH >8 to cause visible surface changes.
- Material damage such as corrosion, cracks, fracturing, premature aging, or swelling.
- Do not use metal cleaning brushes or other abrasives that would damage the product surfaces and could cause corrosion.
- Further detailed advice on hygienically safe and material-/value-preserving reprocessing can be found at www.a-k-i.org, link to “AKI-Brochures”, “Red brochure”.
Reusable products
Influences of the reprocessing which lead to damage to the product are not known. A careful visual and functional inspection before the next use is the best opportunity to recognize a product that is no longer functional, see Inspection.
Preparations at the place of use
- If applicable, rinse non-visible surfaces preferably with deionized water, with a disposable syringe for example.
- Remove any visible surgical residues to the extent possible with a damp, lint-free cloth.
- Transport the dry product in a sealed waste container for cleaning and disinfection within 6 hours.
Cleaning/Disinfection
- Product-specific safety information on the reprocessing method
- Damage to or destruction of the product due to inappropriate cleaning/disinfecting agents and/or excessive temperatures!
- Use cleaning agents and disinfectants according to the manufacturer’s instructions.
- Observe specifications regarding concentration, temperature,e and exposure time.
- Do not exceed a disinfection temperature of 96 °C.
- For products with plasma layers (e.g. Noir instruments), the layer can be damaged or worn if special cleaning procedures with oxidizing chemicals (e.g. hydrogen peroxide H2O2) are used.
- Do not use oxidizing chemicals for cleaning.
- For wet disposal, use suitable cleaning agents/disinfectants. To prevent foam formation and reduced effectiveness of the process chemicals: Before mechanical cleaning and disinfection, rinse the product thoroughly under running water Validated cleaning and disinfection procedure.
Manual cleaning/disinfection
- Before manual disinfecting, allow water to drip off for a sufficient length of time to prevent dilution of the disinfecting solution.
- After manual cleaning/disinfection, check visible surfaces visually for residues.
- Repeat the cleaning/disinfection process if necessary.
Manual cleaning with immersion disinfection
- D–W: Drinking water
- FD–W: Fully desalinated water (demineralized, low microbiological contamination: drinking water quality at least)
- RT: Room temperature
Recommended: BBraun Stabimed fresh
- Note the information on appropriate cleaning brushes and disposable syringes, see Validated cleaning and disinfection procedure.
Phase I
- Fully immerse the product in the cleaning/disinfectant for at least 15 min. Ensure that all accessible surfaces are moistened.
- Clean the product with a suitable cleaning brush in the solution until all discernible residues have been removed from the surface.
- If applicable, brush through non-visible surfaces with an appropriate cleaning brush for at least 1 minute.
- Mobilize non-rigid components, such as set screws, links, etc. during cleaning.
- Thoroughly rinse through these components with the cleaning disinfectant solution (at least five times), using a disposable syringe.
Phase II
- Rinse/flush the product thoroughly (all accessible surfaces) under running water.
- Mobilize non-rigid components, such as set screws, joints, etc. during rinsing.
- Drain any remaining water fully.
Phase III
- Fully immerse the product in the disinfectant solution.
- Mobilize non-rigid components, such as set screws, joints, etc. during rinsing.
- Rinse lumens at least 5 times at the beginning of the exposure time using an appropriate disposable syringe.
- Ensure that all accessible surfaces are moistened.
Phase IV
- Rinse/flush the product thoroughly (all accessible surfaces).
- Mobilize non-rigid components, such as set screws, joints, etc. during the final rinse.
- Rinse lumens with an appropriate disposable syringe at least five times.
- Drain any remaining water fully.
Phase V
- Dry the product in the drying phase with suitable equipment (e.g. cloth, compressed air), see Validated cleaning and disinfection procedure.
Mechanical cleaning/disinfection
Note
The cleaning and disinfection device must be of tested and approved effectiveness (e.g. FDA approval or CE mark according to DIN EN ISO 15883).
Note
The cleaning and disinfection device used for processing must be serviced and checked at regular intervals.
Mechanical alkaline cleaning and thermal disinfection
Machine type: single-chamber cleaning/disinfection device without ultrasound.
D–W: Drinking water
- FD–W: Fully desalinated water (demineralized, low microbiological contamination: drinking water quality at least)
- Recommended: BBraun Helimatic Cleaner alkaline
- Check visible surfaces for residues after mechanical cleaning/disinfecting.
Inspection
- Allow the product to cool down to room temperature.
- Dry the product if it is wet.
Visual inspection
- Make sure all dirt has been removed. In particular, pay attention to, for example, mating surfaces, hinges, shafts, recessed areas, and drilled grooves.
- If the product is dirty: repeat the cleaning and disinfection process.
- Check the product for damage, e.g., corroded, loose, bent, broken, cracked, worn, heavily scratched,d, or missing parts.
- Check the product for missing or faded labels.
- Check the cutting edges for continuity, sharpness, nicks, and other damage.
- Check the surfaces for rough spots.
- Check the product for burrs that could damage tissue or surgical gloves.
- Check the product for loose or missing parts.
- Immediately put aside damaged or inoperative products and send them to Aesculap Technical Service, see Technical Service.
Functional test
CAUTION
Damage (metal cold welding/friction corrosion) to the product caused by insufficient lubrication!
- Before function checks, lubricate moving parts (e.g. joints, pusher components, and threaded rods) with maintenance oil suitable for the respective sterilization process (e.g. for steam sterilization: STERILIT® I oil spray JG600 or STERILIT® I drip lubricator JG598).
- Check that the product functions correctly.
- Check that all moving parts are working properly (e.g. hinges, locks/latches, sliding parts, etc.).
- Make sure that the scissor blades provide light resistance when closing.
- Immediately put aside inoperative products and send them to Aesculap Technical Service, see TechnicalServicee.
Packaging
- Appropriately protect products with fine working tips.
- Place the product in its holder or on a suitable tray. Ensure that sharp edges are covered.
- Package trays appropriately for the sterilization process (e.g. in Aesculap sterile containers).
- Ensure that the packaging provides sufficient protection against contamination of the product during storage.
Steam sterilization
- Check to ensure that the sterilizing agent will come into contact with all external and internal surfaces (e.g., by opening any valves and faucets).
- Validated sterilization process
- Steam sterilization in fractionated vacuum process
- Steam sterilizer by DIN EN 285 and validated by DIN EN ISO 17665
- sterilization in fractionated vacuum process at 134 °C, holding time 5 min
- If several devices are sterilized at the same time in the same steam sterilizer: Ensure that the maximum permitted load according to the manufacturer’s specifications is not exceeded.
Storage
Store sterile products in germ-proof packaging, protected from dust, in a dry, dark, temperature-controlled area.
Technical service
CAUTION
Modifications carried out on medical technical equipment may result in loss of guarantee/warranty rights and forfeiture of applicable licenses.
- Do not modify the product.
- For service and repairs, please contact your national B. Braun/Aesculap agency.
Service addresses
Aesculap Technischer Service
Am Aesculap-Platz
78532 Tuttlingen / Germany
Phone: +49 7461 95-1601
Fax: +49 7461 16-2887
E-Mail: ats@aesculap.de
Other service addresses can be obtained from the address indicated above.
Disposal
WARNING
Risk of infection due to contaminated products! Adhere to national regulations when disposing of or recycling the product, its components, and its packaging.
WARNING
Risk of injury due to sharp-edged and/or pointed products! When disposing of or recycling the product, ensure that the packaging prevents injury to the product.
Note
The user institution is obliged to reprocess the product before its disposal, see Validated reprocessing procedure. TA015820 2021-01 Change No. 63662
Documents / Resources
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Aesculap M39101BG Ring Type Scissors and Spring [pdf] Instructions TA015820, M39101BG, M39101BG Ring Type Scissors and Spring, M39101BG, Ring Type Scissors and Spring, Type Scissors and Spring, Scissors and Spring, Spring |
