Taiwan FDA registration 36a056e3d5e6e2d1c40bcaf16a9a25c5
"Plasmatec" Salmonella Antigen Rapid Test (Non-sterile)
TW: "醫誠"沙門氏菌抗原檢測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·LAB 21 HEALTHCARE LTD·Registered Feb 03, 2020 – Feb 03, 2025ExpiredRegistration details
- Analysis ID
- 36a056e3d5e6e2d1c40bcaf16a9a25c5
- License Form
- Ministry of Health Medical Device Import No. 021223
- Customs Code
- DHA09402122300
Company information
- Manufacturer
- LAB 21 HEALTHCARE LTD
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EUGENE-CHEN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Salmonella Serological Reagent (C.3550)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3550 Salmonella serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 03, 2020
- Expiry Date
- Feb 03, 2025
About this record
Access comprehensive regulatory information for "Plasmatec" Salmonella Antigen Rapid Test (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 36a056e3d5e6e2d1c40bcaf16a9a25c5 and manufactured by LAB 21 HEALTHCARE LTD. The authorized representative in Taiwan is EUGENE-CHEN 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