5°C
70%
45%
35°C
Akces-MED Ltd.
reserve the right to introduce technical and trading changes in
the content of the instruction without warning.
Manufacturer takes responsibility for proper usage of the device only when
the product was purchased from qualified
Akces-MED Ltd.
employee or
at specialized medical store!
Product marked with the CE sign is Class I medical device, of rule 1, consistent with
the requirements of Regulation (EU) 2017/745 of the European Parliament and of
the Council of 5 April 2017 on medical devices.
Akces-Med Ltd.
Company introduced quality management system ISO 13485 regarding
production, sales and service. The system is certified by Det Norske Veritas.
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