Taiwan FDA registration d63425c08fedf706b2f2d4bc92385f44
Karma Air cushion(Non-Sterile)
TW: 康揚氣墊(未滅菌)
Registration details
- Analysis ID
- d63425c08fedf706b2f2d4bc92385f44
- License Form
- Ministry of Health Medical Device Import No. 020711
- Customs Code
- DHA09402071105
Company information
- Manufacturer
- VICAIR BV
- Manufacturer Country
- Netherlands
- Authorized Representative
- KARMA MEDICAL PRODUCTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3175 floating seat cushion
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 01, 2019
- Expiry Date
- Aug 01, 2024
About this record
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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