Taiwan FDA registration 7d117bfcedfe5f2d21680e69ccc40190
Bioken Immunosphere Protein M Tester
TW: 生研免疫球蛋白M試劑
Taiwan·Risk Class 2·DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY·Registered Oct 14, 2005 – Oct 14, 2020CancelledRegistration details
- Analysis ID
- 7d117bfcedfe5f2d21680e69ccc40190
- Customs Code
- DHA00601317901
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Measure the level of immunoglobulin M (IgM) in serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Import Information
- import
Dates and status
- Registration Date
- Oct 14, 2005
- Expiry Date
- Oct 14, 2020
- Cancellation Date
- Aug 18, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Bioken Immunosphere Protein M Tester in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d117bfcedfe5f2d21680e69ccc40190 and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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