Taiwan FDA registration e66e806c2e714c8d68c8512bbeae0c2e
Nofafer Human Mumps Virus Immunoglobulin G Enzyme Immunoassay Kit (Unsterilized)
TW: 諾法鐵人類抗腮腺炎病毒免疫球蛋白G酵素免疫分析套組(未滅菌)
Taiwan·Risk Class 1·GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH·Registered Mar 16, 2006 – Mar 16, 2026ExpiredRegistration details
- Analysis ID
- e66e806c2e714c8d68c8512bbeae0c2e
- Customs Code
- DHA04400297900
Company information
- Manufacturer
- GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- Qualitative detection of anti-mumps virus immunoglobulin G antibodies in human serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3380 腮腺炎病毒血清試劑
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 16, 2006
- Expiry Date
- Mar 16, 2026
About this record
Access comprehensive regulatory information for Nofafer Human Mumps Virus Immunoglobulin G Enzyme Immunoassay Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e66e806c2e714c8d68c8512bbeae0c2e and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) 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