"PRF" Automated sedimentation rate device (NON-STERILE)
Taiwan·Risk Class 1·MD·PROCESS FOR PRF S.A.R.L·Registered Jul 21, 2016 – Jul 21, 2026Expired- Analysis ID
- 70849deac162543c35a4dc3373231374
- License Form
- Ministry of Health Medical Device Import No. 016794
- Customs Code
- DHA09401679407
- Manufacturer
- PROCESS FOR PRF S.A.R.L
- Manufacturer Country
- France
- Authorized Representative
- A SUN TECHNOLOGY 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
- Jul 21, 2016
- Expiry Date
- Jul 21, 2026
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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 70849deac162543c35a4dc3373231374 and manufactured by PROCESS FOR PRF S.A.R.L. The authorized representative in Taiwan is A SUN TECHNOLOGY 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.