Taiwan FDA registration 3d33a62afc67787a07b1fe0d3e5795c0
Nofaferric Human Mumps Virus Immunoglobulin M Enzyme Immunoassay Kit (Unsterilized)
TW: 諾法鐵人類抗腮腺炎病毒免疫球蛋白M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
- 3d33a62afc67787a07b1fe0d3e5795c0
- Customs Code
- DHA04400297709
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 class M 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 Nofaferric Human Mumps Virus Immunoglobulin M 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 3d33a62afc67787a07b1fe0d3e5795c0 and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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