Taiwan FDA registration 7ac5437c77ba33f6b893d65282ec6c26
DiaClon Anti-B
TW: “伯瑞” 單株抗體抗B型鑑定試劑
Taiwan·Risk Class 3·MD·DIAMED GMBH·Registered Feb 21, 2019 – Feb 21, 2029ActiveRegistration details
- Analysis ID
- 7ac5437c77ba33f6b893d65282ec6c26
- License Form
- Ministry of Health Medical Device Import No. 032180
- Customs Code
- DHA05603218009
Company information
- Manufacturer
- DIAMED GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
Product details
- Intended Use
- This product contains a single strain of IgM antibody, which can be used for B blood group typing by slide or test tube method.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B4020 Analyze specific reagents
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 21, 2019
- Expiry Date
- Feb 21, 2029
About this record
Access comprehensive regulatory information for DiaClon Anti-B in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7ac5437c77ba33f6b893d65282ec6c26 and manufactured by DIAMED GMBH. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
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