11
Sterilization for the US market
•
Sterilization of the device may be accomplished by
steam.
•
Aesculap does not recommend the device be ster-
ilized by “Flash” or chemical sterilization.
•
Surgical instruments may also be placed within an
Aesculap rigid sterilization container (sterile con-
tainer) for processing under generally accepted
hospital in-use conditions.
The recommended sterilization parameters are as fol-
lows:
WARNING for the US market
If this device is/was used in a patient with, or sus-
pected of having Creutzfeldt-Jakob Disease (CJD),
the device cannot be reused and must be destroyed
due to the inability to reprocess or sterilize to elim-
inate the risk of cross-contamination!
Storage
¾
Store processed products in germ-proof packaging
in a dust-protected, dry, dark and temperature-
controlled room.
Technical Service
For service, maintenance and repairs, please contact
your national B. Braun/Aesculap agency.
Modifications carried out on medical technical
equipment may result in loss of guarantee/warranty
rights and forfeiture of applicable licenses.
Service addresses
Aesculap Technischer Service
Am Aesculap-Platz
78532 Tuttlingen / Germany
Phone:
+49 7461 95-1602
Fax:
+49 7461 16-5621
E-mail:
Or in the US:
Aesculap Inc.
Attn. Aesculap Technical Services
615 Lambert Pointe Drive
Hazelwood, MO 63042
Aesculap Repair Hotline
Phone:
+1 800 214-3392
Fax:
+1 314 895-4420
Other service addresses can be obtained from the
address indicated above.
Distributor in the US/Contact in Canada for
product information and complaints
Aesculap Inc.
3773 Corporate Parkway
Center Valley, PA 18034
USA
Sterilization
method
Temp.
Minimum exposure time
Wrapped
In a sterile
container
system
Pre-vacuum
270—
275 °F
4 min
4 min
Содержание Aesculap Surgical Instruments
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