"PRF" Automated sedimentation rate device (NON-STERILE)
Taiwan·Risk Class 1·MD·PROCESS FOR PRF S.A.R.L·Registered Aug 27, 2015 – Aug 27, 2025Expired- Analysis ID
- dd393b178e9a5b30895529bdf4d006ac
- License Form
- Ministry of Health Medical Device Import No. 015604
- Customs Code
- DHA09401560400
- Manufacturer
- PROCESS FOR PRF S.A.R.L
- Manufacturer Country
- France
- Authorized Representative
- SE-US CO., LTD.
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Automatic Sedimentation Rate Device (B.5800)".
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B5800 Automatic Settling Rate Device
- Import Information
- Imported from abroad
- Registration Date
- Aug 27, 2015
- Expiry Date
- Aug 27, 2025
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Access comprehensive regulatory information for "PRF" Automated sedimentation rate device (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 dd393b178e9a5b30895529bdf4d006ac and manufactured by PROCESS FOR PRF S.A.R.L. The authorized representative in Taiwan is SE-US CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SARL PROCESS FOR PRF, PROCESS FOR PRF S.A.R.L, and 4 recent registrations in the same category. 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.