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EN
1. FOREWORD
GCE microbiological filters are medical devices classified as class I accord-
ing to the Medical Device Directive 93/42/EEC.
Their Compliance with essential requirements of 93/42/EEC Medical De-
vice Directive is based upon EN ISO 10079-3 standard.
2. INTENDED USE
This filter is intended for use in an exhaust system.
The filter shall be connected by mounting it onto the safety jar of a vacuum
regulator.
The filter makes it possible to:
• intercept impurities present in the air and in the sucked liquid,
• protect the vacuum regulator against potential microbial contamination.
3. TECHNICAL DATA
• Material: filter / glass fibre (borosilicate glass) bonded with
a synthetic bonding agent
housing / polypropylene – natural, transparent
• Impurity interception threshold: 0.3 μm
• Weight: 10 g
• Dimensions: filter 50 mm
housing 58 mm
• Outlet connection: diameter 9 x 13 mm
• Inlet connection: for suction hose of internal diameter of 8 to 9 mm.
4. SAFETY MEASURES AND PERSONNEL TRAINING
Upon opening the package, check the product for damage.
In accordance with Medical Device Directive 93/42/EEC, the microbiologi-
cal filter must only be used by trained personnel, who are familiarized with
the instruction for use of the microbiological filter stated herein.
5. OPERATION
5.1. USING THE MICROBIOLOGICAL FILTER
The microbiological filter shall be used together with the Medicollect 100
jars. Each time a patient is changed, GCE recommends replacing the filter
and all the components of the exhaust system that came into contact with
the sucked liquid.
When using it in one patient for several days, conduct a visual check on the
extent of filter clogging. Filter clogging leads to a perceptible decrease in
the suction power. If it is used in one patient on a long-term basis, replace
it at least once a week.
Do not try to open the filter housing!
Do not use the filter repeatedly! In case of repeated use a contamination
and wrong function of the device can happened!