Taiwan FDA registration 048f4ad28833f7d3d7b4de441c057ed9
DiaClon Anti-A
TW: “伯瑞” 單株抗體抗A型鑑定試劑
Taiwan·Risk Class 3·MD·DIAMED GMBH·Registered Feb 13, 2019 – Feb 13, 2029ActiveRegistration details
- Analysis ID
- 048f4ad28833f7d3d7b4de441c057ed9
- License Form
- Ministry of Health Medical Device Import No. 032169
- Customs Code
- DHA05603216908
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 classification of blood group A 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 13, 2019
- Expiry Date
- Feb 13, 2029
About this record
Access comprehensive regulatory information for DiaClon Anti-A in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 048f4ad28833f7d3d7b4de441c057ed9 and manufactured by DIAMED GMBH. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
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