Taiwan FDA registration 6c6eeb0f57b5e1f2f74fc524cb28f80c
and light B composite standard
TW: 和光B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
- 6c6eeb0f57b5e1f2f74fc524cb28f80c
- Customs Code
- DHA00601561005
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- This standard solution with WAKO's reagents can be used to determine the content of glucose, uric acid, and urea nitrogen 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 B 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 6c6eeb0f57b5e1f2f74fc524cb28f80c and manufactured by FUJIFILM Wako Pure Chemical Corporation Mie Plant. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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