Taiwan FDA registration cf3d3fe4ab41d2a95e9e79330e12f049
and light urea nitrogen
TW: 和光尿素氮
Taiwan·Risk Class 2·FUJIFILM Wako Pure Chemical Corporation Mie Plant·Registered Dec 12, 2005 – Dec 12, 2025ExpiredRegistration details
- Analysis ID
- cf3d3fe4ab41d2a95e9e79330e12f049
- Customs Code
- DHA00601550304
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Urea nitrogen in human serum, plasma or urine is digitized using a test-tube colorimetric test.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1770 尿素氮試驗系統
- 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 light urea nitrogen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cf3d3fe4ab41d2a95e9e79330e12f049 and manufactured by FUJIFILM Wako Pure Chemical Corporation Mie Plant. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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