HEINE visionPRO Quick Start Manual

Hygienic reprocessing
HEINE visionPRO video laryngoscope
General warning and safety information
WARNING! This symbol draws attention to a potentially dangerous situation. Failure to
observe it can result in moderate to severe injuries.
NOTE! This symbol is used to indicate information that is important, but not associated with
danger.
The following information on hygienic reprocessing must be implemented in accordance
with national standards, laws, guidelines and recommendations.
The hygienic reprocessing measures described are not a substitute for the regulations
applicable to the establishment in question.
Dispose of the video laryngoscope blade before reprocessing. The blade is a single-use
product and must not be reprocessed and reused under any circumstances.
Where it is suspected that devices have come into contact with Creutzfeld-Jakob disease
(CJD) pathogens or variants thereof, they must not be reprocessed under any
circumstances and must be disposed of.
If you use reprocessing agents that are not described by HEINE, observe the information
provided by the reprocessing agent manufacturer.
HEINE Optotechnik GmbH & Co. KG only approves the recommended agents and
procedures.
Reprocessing may only be carried out by persons with sufficient expertise in hygiene.
HEINE Optotechnik GmbH & Co. KG has validated the effective reprocessing for the
procedures and agents recommended in this document.
If a reprocessing procedure other than that described in these instructions is used, an
approved and validated reprocessing procedure must be carried out. It must be validated
by the user (e.g. the hospital) or the manufacturers of the reprocessing devices.
Use disinfectant solutions that are fungicidal, bactericidal (including against mycobacteria)
and virucidal.
Do not press in the visionPRO's latching balls under water.
During reprocessing, ensure that soiling is removed from the charging pins to guarantee a
good charging function.
Steam sterilisation or automated reprocessing must not be carried out.
The protective case for the display unit (if available) must be removed before
reprocessing.
The display protector must be replaced when treating high-risk patients.
Regularly check the validity of all the information provided by the reprocessing agent
manufacturer.
The reprocessing agents on the MED 236208 list were tested to ensure material
compatibility.
Do not use agents containing hydrogen peroxide.
Do not allow liquids to get into the device.
Reprocessing
restrictions
HEINE Optotechnik GmbH & Co. KG, Dornierstr. 6, 82205 Gilching, Germany
•
Regularly check that the device is intact.
•
Regularly check that the camera and the illumination are working.
•
The display protector must be replaced if damaged.
med 235566 03/04/2024
Email: info@heine.com, www.heine.com
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