Taiwan FDA registration 0be9e60b1a4c5ca5c0a7ae7080a7299a
Xinkang Comprehensive Quality Control Solution (Unsterilized)
TW: 心康綜合品管液 (未滅菌)
Taiwan·Risk Class 1·POLYMER TECHNOLOGY SYSTEMS,INC.·Registered Jun 18, 2009 – Jun 18, 2024ExpiredRegistration details
- Analysis ID
- 0be9e60b1a4c5ca5c0a7ae7080a7299a
- Customs Code
- DHA04400783705
Company information
- Manufacturer
- POLYMER TECHNOLOGY SYSTEMS,INC.
- Manufacturer Country
- United States
- Authorized Representative
- APEX BIOTECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- import
Dates and status
- Registration Date
- Jun 18, 2009
- Expiry Date
- Jun 18, 2024
About this record
Access comprehensive regulatory information for Xinkang Comprehensive Quality Control Solution (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0be9e60b1a4c5ca5c0a7ae7080a7299a and manufactured by POLYMER TECHNOLOGY SYSTEMS,INC.. The authorized representative in Taiwan is APEX BIOTECHNOLOGY CORPORATION.
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