Taiwan FDA registration 081238386c04ac873a00e97a90b6ffba
Fujifilm-assay C-reactive protein dry test piece
TW: 富士-測定 C-反應蛋白乾式試片
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Dec 13, 2005 – Dec 13, 2025ExpiredRegistration details
- Analysis ID
- 081238386c04ac873a00e97a90b6ffba
- Customs Code
- DHA00601555500
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Serum C-reactive protein concentration is measured.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5270 C反應蛋白免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Dec 13, 2005
- Expiry Date
- Dec 13, 2025
About this record
Access comprehensive regulatory information for Fujifilm-assay C-reactive protein dry test piece in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 081238386c04ac873a00e97a90b6ffba and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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