Taiwan FDA registration 39154efa9e651cd0b163bcd3a02ab2a0
“EUROIMMUN” Anti-Glutamate receptor (type NMDA) IIFT
TW: “歐蒙” 免疫螢光法抗麩胺酸受體(NMDA)抗體檢測試劑
Taiwan·Risk Class 2·MD·EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG·Registered Jun 12, 2018 – Jun 12, 2028ActiveRegistration details
- Analysis ID
- 39154efa9e651cd0b163bcd3a02ab2a0
- License Form
- Ministry of Health Medical Device Import No. 031145
- Customs Code
- DHA05603114502
Company information
- Manufacturer
- EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG
- Manufacturer Country
- Germany
- Authorized Representative
- EUROIMMUN (SOUTH EAST ASIA) PTE. LTD. TAIWAN BRANCH (SINGAPORE)
Product details
- Intended Use
- This product is used for in vitro qualitative or semi-quantitative detection of anti-glutaminate receptor (NMDA type) antibody immunoglobulin IgG antibodies in human serum, plasma or cerebrospinal fluid (CSF) samples.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C5660 Multiple autologous antibody immunoassay system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 12, 2018
- Expiry Date
- Jun 12, 2028
About this record
Access comprehensive regulatory information for “EUROIMMUN” Anti-Glutamate receptor (type NMDA) IIFT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 39154efa9e651cd0b163bcd3a02ab2a0 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is EUROIMMUN (SOUTH EAST ASIA) PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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