Taiwan FDA registration 208253ba1de7ce854ea600aaf380437f
Reagent for the determination of electrolyte in water
TW: 積水電解質測定試劑
Taiwan·Risk Class 2·SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT·Registered Dec 19, 2005 – Dec 19, 2025ExpiredRegistration details
- Analysis ID
- 208253ba1de7ce854ea600aaf380437f
- Customs Code
- DHA00601564307
Company information
- Manufacturer
- SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- KUO'S YUAN IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Determination of serum or plasma sodium (Na), potassium (K+), chlorine (Cl-).
- 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 19, 2005
- Expiry Date
- Dec 19, 2025
About this record
Access comprehensive regulatory information for Reagent for the determination of electrolyte in water in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 208253ba1de7ce854ea600aaf380437f and manufactured by SEKISUI MEDICAL CO., LTD. TSUKUBA PLANT. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices