neoprobe
TM
GDS Operation Manual
AW-000639
Page
23 of 38
Reprocessing of Power Cord according to EN ISO 17664:2004
Manufacturer:
Devicor Medical Products, Inc.
300 E-Business Way, Fifth Floor
Cincinnati, OH 45241-2378 USA
Method: Cleaning & Disinfection
Symbol:
Model 2009
Devices(s):
Reusable power cords comprising fixed assemblies (no moving parts); sold nonsterile.
WARNING:
WARNING
: disconnect power cord from power source before cleaning to avoid
electrical shock.
Limitations on
reprocessing:
Repeated processing has little effect on cable. End of life is normally determined by
abrasion, wear and damage due to use.
INSTRUCTIONS:
Point of use
:
Remove excess soil and surface contamination with disposable cloth/paper wipe.
Containment &
Transportation
:
No particular requirements. Recommend reprocessing instrument soon after surgical use.
Preparation for
cleaning
:
WARNING
: disconnect power cord from power source before cleaning to avoid
electrical shock
Cleaning - Automated
:
Do not use automated cleaning. Clean by hand; cleaning instructions below.
Cleaning: Manual
Equipment: mild detergent and lint free cloth.
Method:
1.
Dampen cloth with mild detergent and wipe excess soil from surface
2.
Visually inspect for cleanliness
3.
Repeat steps 1 to 3 until visually clean.
4.
Allow to dry in room air
Disinfection:
No requirement
Drying:
Air dry at room temperature
Maintenance:
Do not use worn, cracked or damaged cable
Inspection & Function
Testing:
All instruments: Visually inspect for damage or wear. Where cable forms part of a larger
assembly, check assembly with mating components.
Packaging:
No requirement
Sterilization:
Power cord does not require sterilization
Storage:
No requirement
Additional Information:
Periodically perform safety test with equipment system to assure continued integrity of
power cord.
Manufacturer Contact:
See troubleshooting section for telephone and address of local representative or telephone
1-877-926-2666
.
NOTE
: Instructions provided above are validated by medical device manufacturer as being capable of preparing a
medical device for re-use. It remains responsibility of reprocessor to ensure that reprocessing is actually performed using
equipment, materials, and personnel in processing facility to achieve desired result. This requires validation and routine
monitoring of processes. Likewise any deviation by processor from instructions provided should be properly evaluated for
effectiveness and potential adverse consequences.
Artwork No: AW-000639 Revision: A Artwork Status: Released Lifecycle Name: Artwork
PCO No: N/A ECN No: ECN-000214 Release Date: 10/09/2012 Effective Date: 10/09/2012
