"PRF" Automated Sedimentation Rate Device (Non-Sterile)
Taiwan·Risk Class 1·MD·SARL PROCESS FOR PRF·Registered Dec 15, 2017 – Dec 15, 2022Expired- Analysis ID
- 470e8c10f5360c3f7b2850acd158e071
- License Form
- Ministry of Health Medical Device Import No. 018619
- Customs Code
- DHA09401861902
- Manufacturer
- SARL PROCESS FOR PRF
- Manufacturer Country
- France
- Authorized Representative
- HON INTERNATIONAL TRADING 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
- Dec 15, 2017
- Expiry Date
- Dec 15, 2022
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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 470e8c10f5360c3f7b2850acd158e071 and manufactured by SARL PROCESS FOR PRF. The authorized representative in Taiwan is HON INTERNATIONAL TRADING 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.