Taiwan FDA registration b6d6f3c46bde6a22b091346fdbca2371
and photomagnesium test system (unsterilized)
TW: 和光鎂試驗系統(未滅菌)
Taiwan·Risk Class 1·FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT·Registered Oct 25, 2005 – Oct 25, 2025ExpiredRegistration details
- Analysis ID
- b6d6f3c46bde6a22b091346fdbca2371
- Customs Code
- DHA04400118306
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Magnesium concentrations in serum and urine are measured.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1495 Magnesium testing system
- Import Information
- import
Dates and status
- Registration Date
- Oct 25, 2005
- Expiry Date
- Oct 25, 2025
About this record
Access comprehensive regulatory information for and photomagnesium test system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b6d6f3c46bde6a22b091346fdbca2371 and manufactured by FUJIFILM WAKO PURE CHEMICAL CORPORATION MIE PLANT. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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