Taiwan FDA registration 419c2de75e51041bb9193e8ef8278eaf
"FUJI" DRICHEM IMMUNO AG FluAB (Non-Sterile)
TW: "富士" 乾式免疫流感(AB)試劑 (未滅菌)
Taiwan·Risk Class 1·MD·FUJIFILM CORPORATION·Registered Jan 09, 2017 – Jan 09, 2022ExpiredRegistration details
- Analysis ID
- 419c2de75e51041bb9193e8ef8278eaf
- License Form
- Ministry of Health Medical Device Import No. 017386
- Customs Code
- DHA09401738600
Company information
- Manufacturer
- FUJIFILM CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
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
- Jan 09, 2017
- Expiry Date
- Jan 09, 2022
About this record
Access comprehensive regulatory information for "FUJI" DRICHEM IMMUNO AG FluAB (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 419c2de75e51041bb9193e8ef8278eaf and manufactured by FUJIFILM CORPORATION. The authorized representative in Taiwan is HUNG CHONG CORP..
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