Taiwan FDA registration cc36c83c286d5de477030cbd6370993d
"Kipfu" General Internal Control Group (Non-sterile)
TW: "基普復" 泛用內部控制組(未滅菌)
Registration details
- Analysis ID
- cc36c83c286d5de477030cbd6370993d
- Customs Code
- DHA09402336106
Company information
- Manufacturer
- GeneProof a. s.
- Manufacturer Country
- Czechia
- Authorized Representative
- MEDTRI CO., LTD.
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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jan 15, 2024
- Expiry Date
- Jan 15, 2029
About this record
Access comprehensive regulatory information for "Kipfu" General Internal Control Group (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 cc36c83c286d5de477030cbd6370993d and manufactured by GeneProof a. s.. 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