Taiwan FDA registration c76c63de7ae01d880ae340b53dcebbae
“ARKRAY” Standard Solution Set
TW: “愛科來” 滲透壓標準液組
Taiwan·Risk Class 2·MD·ARKRAY FACTORY, INC.·Registered Nov 18, 2016 – Nov 18, 2026ActiveRegistration details
- Analysis ID
- c76c63de7ae01d880ae340b53dcebbae
- License Form
- Ministry of Health Medical Device Import No. 028953
- Customs Code
- DHA05602895300
Company information
- Manufacturer
- ARKRAY FACTORY, INC.
- Manufacturer Country
- Japan
- Authorized Representative
- MEDTRI CO., LTD.
Product details
- Intended Use
- This standard set is limited to use as a standard solution for AGCO osmotic analyzers.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1150 calibrate
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 18, 2016
- Expiry Date
- Nov 18, 2026
About this record
Access comprehensive regulatory information for “ARKRAY” Standard Solution Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c76c63de7ae01d880ae340b53dcebbae and manufactured by ARKRAY FACTORY, INC.. The authorized representative in Taiwan is MEDTRI 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