Taiwan FDA registration dfe1257461595799e1475df6520ac70c
“Bio-Rad” Control Card A
TW: “伯瑞” 品管卡片
Taiwan·Risk Class 2·MD·DIAMED GMBH·Registered Dec 12, 2018 – Dec 12, 2028ActiveRegistration details
- Analysis ID
- dfe1257461595799e1475df6520ac70c
- License Form
- Ministry of Health Medical Device Import No. 031962
- Customs Code
- DHA05603196208
Company information
- Manufacturer
- DIAMED GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
Product details
- Intended Use
- With DiaClon Anti-CW and DiaClon Rh-Subgroups+CW +K negative quality control materials suitable for manual and instrumental ID cards.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9650 Quality control equipment for blood bank reactors
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 12, 2018
- Expiry Date
- Dec 12, 2028
About this record
Access comprehensive regulatory information for “Bio-Rad” Control Card A in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dfe1257461595799e1475df6520ac70c 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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