Taiwan FDA registration 68f29ff245b6e9499ea8049aa93319f5
"Bioresearch" Listeria antiserum kit (unsterilized)
TW: “生研”李司特氏菌屬抗血清試劑套組(未滅菌)
Taiwan·Risk Class 1·DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY·Registered Feb 22, 2012 – Feb 22, 2022CancelledRegistration details
- Analysis ID
- 68f29ff245b6e9499ea8049aa93319f5
- Customs Code
- DHA04401140109
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Listeria sera reagent (C.3355)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3355 李斯特氏菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Feb 22, 2012
- Expiry Date
- Feb 22, 2022
- Cancellation Date
- Jun 30, 2022
Cancellation information
- Status
- Logged out
- Reason
- 屆期未申請展延;;自請註銷
About this record
Access comprehensive regulatory information for "Bioresearch" Listeria antiserum kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 68f29ff245b6e9499ea8049aa93319f5 and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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