Taiwan FDA registration 9ad4d7f4cb97f3e35cebc149ff0ebdac
and light A composite standard
TW: 和光A複合式標準液
Taiwan·Risk Class 2·FUJIFILM Wako Pure Chemical Corporation Mie Plant·Registered Dec 16, 2005 – Dec 16, 2025ExpiredRegistration details
- Analysis ID
- 9ad4d7f4cb97f3e35cebc149ff0ebdac
- Customs Code
- DHA00601560805
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- This standard solution with WAKO reagents can be used to determine the levels of calcium, iron, magnesium, and inorganic phosphorus in human serum, plasma, or urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Dec 16, 2005
- Expiry Date
- Dec 16, 2025
About this record
Access comprehensive regulatory information for and light A composite standard in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ad4d7f4cb97f3e35cebc149ff0ebdac and manufactured by FUJIFILM Wako Pure Chemical Corporation Mie Plant. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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