Taiwan FDA registration 308d6e98ab4697d9ede0d18f213ded83
DiaClon Anti-P1
TW: “伯瑞” 單株抗體抗P1血清試劑
Taiwan·Risk Class 2·MD·DIAMED GMBH·Registered May 31, 2016 – May 31, 2026ExpiredRegistration details
- Analysis ID
- 308d6e98ab4697d9ede0d18f213ded83
- License Form
- Ministry of Health Medical Device Import No. 028435
- Customs Code
- DHA05602843501
Company information
- Manufacturer
- DIAMED GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
Product details
- Intended Use
- An antigen-antibody reaction is used to detect the P1 antigen on 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
- May 31, 2016
- Expiry Date
- May 31, 2026
About this record
Access comprehensive regulatory information for DiaClon Anti-P1 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 308d6e98ab4697d9ede0d18f213ded83 and manufactured by DIAMED GMBH. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
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