Taiwan FDA registration 51fdd97b5f97c77acba72bd246946e18
Veromsilon Parainfluenza Virus Type II Complement Kit (unsterilized)
TW: 維隆希隆副流行性感冒病毒二型補體試劑組(未滅菌)
Taiwan·Risk Class 1·INSTITUT VIRIONSERION GMBH·Registered Mar 27, 2006 – Mar 27, 2016CancelledRegistration details
- Analysis ID
- 51fdd97b5f97c77acba72bd246946e18
- Customs Code
- DHA04400319306
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 parainfluenza virus type 2 antibody 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 II 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 51fdd97b5f97c77acba72bd246946e18 and manufactured by INSTITUT VIRIONSERION GMBH. The authorized representative in Taiwan is UNISYS BIOMEDICAL CO..
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