Taiwan FDA registration c7c351bcabddda4324e8c066d70a75ff
Veromsilon parainfluenza virus type 3 complement kit (unsterilized)
TW: 維隆希隆副流行性感冒病毒三型補體試劑組(未滅菌)
Taiwan·Risk Class 1·INSTITUT VIRIONSERION GMBH·Registered Mar 27, 2006 – Mar 27, 2016CancelledRegistration details
- Analysis ID
- c7c351bcabddda4324e8c066d70a75ff
- Customs Code
- DHA04400319204
Company information
- Manufacturer
- INSTITUT VIRIONSERION GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- UNISYS BIOMEDICAL CO.
Product details
- Intended Use
- It is used to measure the concentration of antibodies to parainfluenza virus type 3 in serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3400 Parainfluenza Virus Seroblast
- Import Information
- import
Dates and status
- Registration Date
- Mar 27, 2006
- Expiry Date
- Mar 27, 2016
- Cancellation Date
- May 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Veromsilon parainfluenza virus type 3 complement 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 c7c351bcabddda4324e8c066d70a75ff and manufactured by INSTITUT VIRIONSERION GMBH. The authorized representative in Taiwan is UNISYS BIOMEDICAL CO..
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