Taiwan FDA registration b7d519e6783c14d73b800c809a20c2a1
"Bio-Rad" Potentiating media for in vitro diagnostic use (non-sterile)
TW: "伯瑞" 體外診斷用的強化培養基 (未滅菌)
Taiwan·Risk Class 1·MD·DIAMED GMBH·Registered Jan 11, 2018 – Jan 11, 2028ActiveRegistration details
- Analysis ID
- b7d519e6783c14d73b800c809a20c2a1
- License Form
- Ministry of Health Medical Device Import No. 018713
- Customs Code
- DHA09401871304
Company information
- Manufacturer
- DIAMED GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)
Product details
- Intended Use
- Limited to the first level identification range of intensive medium (B.9600) for in vitro diagnosis of medical device management methods.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9600 Fortified medium for in vitro diagnostics
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 11, 2018
- Expiry Date
- Jan 11, 2028
About this record
Access comprehensive regulatory information for "Bio-Rad" Potentiating media for in vitro diagnostic use (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b7d519e6783c14d73b800c809a20c2a1 and manufactured by DIAMED GMBH. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).
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