"PRF" Automated Sedimentation Rate Device (Non-Sterile)
Taiwan·Risk Class 1·MD·SARL PROCESS FOR PRF·Registered Mar 11, 2016 – Mar 11, 2021Expired- Analysis ID
- 223d1aaf9446c6544f9b896bee7db7bd
- License Form
- Ministry of Health Medical Device Import No. 016247
- Customs Code
- DHA09401624704
- Manufacturer
- SARL PROCESS FOR PRF
- Manufacturer Country
- France
- Authorized Representative
- ADENT MED 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
- Mar 11, 2016
- Expiry Date
- Mar 11, 2021
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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 223d1aaf9446c6544f9b896bee7db7bd and manufactured by SARL PROCESS FOR PRF. The authorized representative in Taiwan is ADENT MED 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.