Stryker Precision AC Bedienungsanleitung Seite 9

Materials and Equipment
All materials and equipment required to reprocess the coupler shall be
supplied by the user unless otherwise noted.
Item
All phases
Gloves, eye protection,
etc.
Cleaning
Tray
Water basin
Enzymatic detergent
Tap water
Syringe
Soft-bristed brush
Reverse osmosis/
deionized water
Clean cloth or filtered
pressurized air
Non-enzymatic
detergent
4
Automated washer
Disinfection
Washer disinfector
Sterilization
Sterilization system
Sterilization wrap
Sterilization tray
1
Cleaning was validated using Enzol® Enzymatic Detergent at 1 oz/gal.
2
Cleaning was validated using an M16 brush.
3
Cleaning was validated using reverse osmosis/deionized (RO/DI) water.
4
Cleaning was validated using Prolystica® 2x Neutral Detergent at 1/8 oz/gal.
5
Sterilization was validated using Kimberly-Clark® KC600 KIMGUARD sterilization wrap.
6
For United States users: when sterilizing the device, use only sterilization wraps and sterilization trays that have
been cleared by the FDA to use with the selected sterilization cycle.
Description
Wear protective equipment as required
by the medical facility and procedure.
For safe transportation of device within
the medical facility. Not to be used for
reprocessing the device unless sterilized
first.
Large enough to accommodate device
Used in cleaning solution to remove
1
surgical debris
To prepare cleaning solutions
Minimum volume: 50 mL
To clean exterior of device
2
To rinse device
3
To assist with drying
Used in cleaning solution to remove
surgical debris
For using the automated cleaning
procedure
To perform thermal disinfection
• Steam (Autoclave)
• Steris®/Amsco® V-PRO® maX, V-PRO 1
Plus, or V-PRO 1
• Sterrad® 100S, 200, NX®, or 100NX®
To maintain sterile barrier
5, 6
Optional. Must be compatible with
6
sterilization method.
EN-5