Taiwan FDA registration 850f1630c981b25eb73be3e8c751a1c2
"Bioken" Krivour Adenovirus (Respiratory) Rapid Test Kit (Unsterilized)
TW: "生研" 快納威 腺病毒(呼吸道)快速檢驗套組 (未滅菌)
Taiwan·Risk Class 1·DENKA CO., LTD·Registered Jun 28, 2012 – Jun 28, 2027ActiveRegistration details
- Analysis ID
- 850f1630c981b25eb73be3e8c751a1c2
- Customs Code
- DHA04401189406
Company information
- Manufacturer
- DENKA CO., LTD
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management method of medical equipment "adenovirus serum reagent (C.3020)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3020 腺病毒血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Jun 28, 2012
- Expiry Date
- Jun 28, 2027
About this record
Access comprehensive regulatory information for "Bioken" Krivour Adenovirus (Respiratory) Rapid Test 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 850f1630c981b25eb73be3e8c751a1c2 and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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