Taiwan FDA registration ee3aa6b0602ae0461129bfb713f833fe
“Sysmex” Revohem ADP
TW: “西森美康”二磷酸腺苷檢測試劑
Taiwan·Risk Class 2·MD·HYPHEN BioMed·Registered Nov 06, 2018 – Nov 06, 2028ActiveRegistration details
- Analysis ID
- ee3aa6b0602ae0461129bfb713f833fe
- License Form
- Ministry of Health Medical Device Import No. 031777
- Customs Code
- DHA05603177700
Company information
- Manufacturer
- HYPHEN BioMed
- Manufacturer Country
- France
- Authorized Representative
- SYSMEX TAIWAN CO., LTD.
Product details
- Intended Use
- This product is used for the detection of platelet agglutination.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B5700 Automated platelet agglutination system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 06, 2018
- Expiry Date
- Nov 06, 2028
About this record
Access comprehensive regulatory information for “Sysmex” Revohem ADP in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ee3aa6b0602ae0461129bfb713f833fe and manufactured by HYPHEN BioMed. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices