Taiwan FDA registration aa84d02bb8f86f813c473a7a67a2ef46
"Shino -Test" Control Solution (Non-sterile)
TW: "篠原" 品管液 (未滅菌)
Taiwan·Risk Class 1·MD·SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER·Registered Apr 15, 2016 – Apr 15, 2026ExpiredRegistration details
- Analysis ID
- aa84d02bb8f86f813c473a7a67a2ef46
- License Form
- Ministry of Health Medical Device Import No. 016408
- Customs Code
- DHA09401640802
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- MEDICARE PRODUCTS INC.
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 15, 2016
- Expiry Date
- Apr 15, 2026
About this record
Access comprehensive regulatory information for "Shino -Test" Control Solution (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aa84d02bb8f86f813c473a7a67a2ef46 and manufactured by SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices