Taiwan FDA registration a873d498d3e07c3e28409d8a52456847
and light microalbumin tube solution automatic instrument set
TW: 和光 微量白蛋白品管液自動儀器套組
Taiwan·Risk Class 2·FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT·Registered Jun 19, 2008 – Jun 19, 2028ActiveRegistration details
- Analysis ID
- a873d498d3e07c3e28409d8a52456847
- Customs Code
- DHA00601938709
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Test tube solution for measuring the amount of urine albumin.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- import
Dates and status
- Registration Date
- Jun 19, 2008
- Expiry Date
- Jun 19, 2028
About this record
Access comprehensive regulatory information for and light microalbumin tube solution automatic instrument set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a873d498d3e07c3e28409d8a52456847 and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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