• Medical Device Regulation 93/42/EEC

Medical Devices Regulation , 93/42/EEC, is CE directive covers the most sensitive products that is Medical Devices, among the devices used for examination, diagnostic, therapeutic purposes, used in our defenceless status and eliminate the health reasoned hazard. 

We, conduct audits by our experienced team for the companies manufacture medical devices remediate you, considering the safety of users is in first place. Kindly look for 2138 ID no next to CE mark for quality in Medical Devices.

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Alberk QA International Technical Control and Certification INC
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