Taiwan FDA registration 35e485f73a38c351fdd82ca0aebfd22c
and photoelectrolyte analysis systems
TW: 和光電解質分析系統
Taiwan·Risk Class 2·FUJIFILM Wako Pure Chemical Corporation Mie Plant·Registered Dec 10, 2005 – Dec 10, 2025ExpiredRegistration details
- Analysis ID
- 35e485f73a38c351fdd82ca0aebfd22c
- Customs Code
- DHA00601545101
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- The electrolyte system with ion selective electrode can determine the content of sodium, potassium and chlorine in human serum or urine using Hitachi biochemical instrument.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1665 Sodium Test System
- Import Information
- import
Dates and status
- Registration Date
- Dec 10, 2005
- Expiry Date
- Dec 10, 2025
About this record
Access comprehensive regulatory information for and photoelectrolyte analysis systems in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 35e485f73a38c351fdd82ca0aebfd22c and manufactured by FUJIFILM Wako Pure Chemical Corporation Mie Plant. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
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