Taiwan FDA registration 22342e644dbbddbc3851b78801b3420a
DENKA Quick Navi-Flu2 (Non-Sterile)
TW: 生研快納威流行性感冒快速檢驗套組第二代(未滅菌)
Taiwan·Risk Class 1·MD·DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY·Registered Nov 21, 2017 – Nov 21, 2022ExpiredRegistration details
- Analysis ID
- 22342e644dbbddbc3851b78801b3420a
- License Form
- Ministry of Health Medical Device Import No. 018531
- Customs Code
- DHA09401853101
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 "Influenza Virus Serum Reagent (C.3330)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3330 Influenza virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 21, 2017
- Expiry Date
- Nov 21, 2022
About this record
Access comprehensive regulatory information for DENKA Quick Navi-Flu2 (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 22342e644dbbddbc3851b78801b3420a and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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