"PRF" Automated Sedimentation Rate Device (Non-Sterile)
Taiwan·Risk Class 1·MD·SARL PROCESS FOR PRF·Registered Sep 17, 2015 – Sep 17, 2020Cancelled- Analysis ID
- 3bc66fb2146d29cc3bc4284a8e409129
- License Form
- Ministry of Health Medical Device Import No. 015683
- Customs Code
- DHA09401568306
- Manufacturer
- SARL PROCESS FOR PRF
- Manufacturer Country
- France
- Authorized Representative
- CONTROL BIOTECH CO., LTD.
- 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
- Sep 17, 2015
- Expiry Date
- Sep 17, 2020
- Cancellation Date
- Jun 22, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期
Top companies providing products similar to ""PRF" Automated Sedimentation Rate Device (Non-Sterile)"
Recently registered similar products
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 3bc66fb2146d29cc3bc4284a8e409129 and manufactured by SARL PROCESS FOR PRF. The authorized representative in Taiwan is CONTROL BIOTECH 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.