at specialized medical store!
Akces-MED. Ltd.
reserve the right to introduce technical and trading changes
in the content of the instruction without warning.
the product was purchased from qualified
Akces-MED Ltd.
employee or
Manufacturer takes responsibility for proper usage of the device only when
5°C
70%
45%
Akces-MED Ltd.
introduced quality management system ISO 13485 regarding
production, sales and service. The system is certified by Det Norske Veritas.
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.
35°C
Summary of Contents for KUKINI
Page 1: ...K U K I N I SPECIAL NEEDS STROLLER USER MANUAL...
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