Taiwan FDA registration a5a17f8a254531eb68d01d74488a0cc9
Bio-research fast Navir Pseudobacterium Serum Test (Unwiped Bacteria)
TW: 生研快納威 黴漿菌屬血清試劑(未滅菌)
Taiwan·Risk Class 1·DENKA CO., LTD·Registered Mar 06, 2024 – Mar 06, 2029ActiveRegistration details
- Analysis ID
- a5a17f8a254531eb68d01d74488a0cc9
- Customs Code
- DHA09402341302
Company information
- Manufacturer
- DENKA CO., LTD
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, the first level identification range of "Mycoplasma serum reagent (C.3375)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3375 黴漿菌屬血清試劑
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 06, 2024
- Expiry Date
- Mar 06, 2029
About this record
Access comprehensive regulatory information for Bio-research fast Navir Pseudobacterium Serum Test (Unwiped Bacteria) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a5a17f8a254531eb68d01d74488a0cc9 and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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