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Karma Air cushion(Non-Sterile) - Taiwan Registration d63425c08fedf706b2f2d4bc92385f44

Access comprehensive regulatory information for Karma Air cushion(Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d63425c08fedf706b2f2d4bc92385f44 and manufactured by VICAIR BV. The authorized representative in Taiwan is KARMA MEDICAL PRODUCTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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d63425c08fedf706b2f2d4bc92385f44
Registration Details
Taiwan FDA Registration: d63425c08fedf706b2f2d4bc92385f44
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Device Details

Karma Air cushion(Non-Sterile)
TW: ๅบทๆšๆฐฃๅขŠ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d63425c08fedf706b2f2d4bc92385f44

Ministry of Health Medical Device Import No. 020711

DHA09402071105

Company Information

Netherlands

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".

o Equipment for physical medicine

O3175 floating seat cushion

Imported from abroad

Dates and Status

Aug 01, 2019

Aug 01, 2024