Taiwan FDA registration 74b8c3b8053dbdb0461274ec15c1a42b
and photoglucose assays
TW: 和光葡萄糖檢驗試劑
Registration details
- Analysis ID
- 74b8c3b8053dbdb0461274ec15c1a42b
- Customs Code
- DHA00601536202
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Quantify glucose content in serum, plasma, or urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1345 Glucose Test System
- Import Information
- import
Dates and status
- Registration Date
- Dec 09, 2005
- Expiry Date
- Dec 09, 2025
About this record
Access comprehensive regulatory information for and photoglucose assays in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 74b8c3b8053dbdb0461274ec15c1a42b and manufactured by FUJIFILM Wako Pure Chemical Corporation Mie Plant. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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