Taiwan FDA registration 0d4de93e7bb99859a012c3de50b175cf
DiaClon Rh-Subgroups+CW+K
TW: “伯瑞” 單株抗體Rh亞型群+CW+K血型鑑定卡片
Taiwan·Risk Class 2·MD·DIAMED GMBH·Registered Oct 05, 2018 – Oct 05, 2028ActiveRegistration details
- Analysis ID
- 0d4de93e7bb99859a012c3de50b175cf
- License Form
- Ministry of Health Medical Device Import No. 031723
- Customs Code
- DHA05603172303
Company information
- Manufacturer
- DIAMED GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
Product details
- Intended Use
- C (RH2), CW (RH8), c (RH4), E (RH3), e (RH5) and K (KEL1) antigens were measured in human red blood cells.
- 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
- Oct 05, 2018
- Expiry Date
- Oct 05, 2028
About this record
Access comprehensive regulatory information for DiaClon Rh-Subgroups+CW+K in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0d4de93e7bb99859a012c3de50b175cf 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.
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