Taiwan FDA registration 3556f32c1754fcccc19c7d83fe1a2dff
Fujifilm-Assay alkaline phosphatase dry test piece
TW: 富士-測定鹼性磷酸酶乾式試片
Taiwan·Risk Class 2·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered Dec 14, 2005 – Dec 14, 2025ExpiredRegistration details
- Analysis ID
- 3556f32c1754fcccc19c7d83fe1a2dff
- Customs Code
- DHA00601556401
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- HUNG CHONG CORP.
Product details
- Intended Use
- Measure the concentration of Alkaline phosphatase in plasma or serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1050 Alkaline phosphatase or isoenzyme testing system
- Import Information
- import
Dates and status
- Registration Date
- Dec 14, 2005
- Expiry Date
- Dec 14, 2025
About this record
Access comprehensive regulatory information for Fujifilm-Assay alkaline phosphatase 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 3556f32c1754fcccc19c7d83fe1a2dff and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..
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