Dräger Primus Infinity Empowered - Classification of Medical Devices; Reprocessing Procedure; Testing of Procedures and Agents; Uncritical Medical Devices

Cleaning, disinfection and sterilization
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Instructions for use Primus Infinity Empowered SW 4.5n
Reprocessing procedure
Classification of medical devices
For reprocessing, the medical products are classi-
fied by their way of application and the risk resulting
from it:
– Uncricital medical devices: surfaces accessible
to users and patients, e.g., device surfaces, ca-
bles
– Semicritical medical devices: parts conducting
breathing gas, e.g., breathing hoses, masks
Testing of procedures and agents
Cleaning, disinfection, and sterilization of medical
devices has been tested with the following proce-
dures and agents. At the time of testing, the follow-
ing procedures and agents showed good material
compatibility and effectiveness:
Uncritical medical devices
Manual disinfection and simultaneous cleaning:
– Incidin Extra N by Ecolab
– Incidur by Ecolab
Semicritical medical devices
Manual cleaning:
– Neodisher Medizym by Dr. Weigert
Manual disinfection:
– Gigasept FF by Schülke & Mayr
Machine cleaning:
– Neodisher Medizym by Dr. Weigert
Machine disinfection:
– Thermal, 93 °C (199.4 °F) for 10 min
Sterilization:
– Hot steam, 134 °C (273.2 °F) for 5 min
Observe corresponding instructions for use. The
medical device may have been tested with other
agents and under other conditions.
Uncritical medical devices
Manual disinfection and simultaneous cleaning
For choosing the appropriate disinfectant, observe
country-specific lists of disinfectants. The list of the
German Association for Applied Hygiene (Verbund
für Angewandte Hygiene VAH) applies in German-
speaking countries.
Strictly observe the manufacturer’s instructions for
using disinfectants. The composition of disinfect-
ants may change.
Procedure:
1 Remove dirt immediately with a wipe soaked in
disinfectant.
2 Perform surface disinfection (scrub-and-wipe
disinfection).
3 After the contact time has elapsed, remove dis-
infectant residues.
WARNING
Risk of electric shock or device malfunction
Penetrating liquid may cause malfunction of
or damage to the device, which may endanger
the patient.
Only scrub-and-wipe-disinfect device sur-
faces and cables and make sure no liquids
penetrate into the device.