12 Medical Device Directives
Components subject to 93/42/EC Medical Devices Directive
All components are designed, manufactured and inspected according to the European
Directive 93/42/EC annex II and art. 11 par. 3.
Overall rating
The purifier unit conform to the Medical Devices Directive 93/42/EC category IIb.
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Содержание dMED 025
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