Taiwan FDA registration 21bdc38f88a2c62b4745e6e01e124b1a
DiaClon Anti-M
TW: "伯瑞" 單株抗體抗M鑑定卡片
Taiwan·Risk Class 2·MD·DIAMED GMBH·Registered Jul 20, 2022 – Jul 20, 2027ActiveRegistration details
- Analysis ID
- 21bdc38f88a2c62b4745e6e01e124b1a
- License Form
- Ministry of Health Medical Device Import No. 035680
- Customs Code
- DHA05603568005
Company information
- Manufacturer
- DIAMED GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
Product details
- Intended Use
- Antigen-antibody response is used to detect M antigen on red blood cells.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B4020 Analyze specific reagents
- Import Information
- Imported from abroad; GMP
Dates and status
- Registration Date
- Jul 20, 2022
- Expiry Date
- Jul 20, 2027
About this record
Access comprehensive regulatory information for DiaClon Anti-M in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 21bdc38f88a2c62b4745e6e01e124b1a and manufactured by DIAMED GMBH. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
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