Taiwan FDA registration f4dd449fa55f9c5b706d6b4665a52d16
and photoalbumin assay reagents
TW: 和光白蛋白測定試劑
Taiwan·Risk Class 2·FUJIFILM Wako Pure Chemical Corporation Mie Plant·Registered Dec 12, 2005 – Dec 12, 2025ExpiredRegistration details
- Analysis ID
- f4dd449fa55f9c5b706d6b4665a52d16
- Customs Code
- DHA00601549801
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Albumin assays use a test-tube colorimetric test to determine the amount of albumin in urine or plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1035 Albumin Testing System
- Import Information
- import
Dates and status
- Registration Date
- Dec 12, 2005
- Expiry Date
- Dec 12, 2025
About this record
Access comprehensive regulatory information for and photoalbumin assay reagents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f4dd449fa55f9c5b706d6b4665a52d16 and manufactured by FUJIFILM Wako Pure Chemical Corporation Mie Plant. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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