Taiwan FDA registration 33ac0667bae343f718ea37da54861853
"Ennegast" herpes simplex virus IgM antibody test reagent
TW: “恩奈格斯特”單純皰疹病毒IgM抗體 檢驗試劑
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Registered Dec 21, 2009 – Dec 21, 2019CancelledRegistration details
- Analysis ID
- 33ac0667bae343f718ea37da54861853
- Customs Code
- DHA00602075502
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Enzyme immunoassay for the qualitative and quantitative detection of herpes simplex virus (HSV) specific IgM antibodies in human serum and plasma.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3305 Seroanalysis of monoperiasis virus
- Import Information
- import
Dates and status
- Registration Date
- Dec 21, 2009
- Expiry Date
- Dec 21, 2019
- Cancellation Date
- Mar 04, 2021
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Ennegast" herpes simplex virus IgM antibody test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 33ac0667bae343f718ea37da54861853 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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