Taiwan FDA registration 6c7fd78e88da9848d4d062c1c334d8c2
Velomsilone pneumoniae complement reagent group
TW: 維隆希隆肺炎黴漿菌補體試劑組
Taiwan·Risk Class 1·INSTITUT VIRIONSERION GMBH·Registered Dec 22, 2005 – Dec 22, 2010CancelledRegistration details
- Analysis ID
- 6c7fd78e88da9848d4d062c1c334d8c2
- Customs Code
- DHA04400231209
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 Pneumobacterium mycosis in serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3375 黴漿菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Dec 22, 2005
- Expiry Date
- Dec 22, 2010
- Cancellation Date
- Jan 21, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Velomsilone pneumoniae complement reagent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6c7fd78e88da9848d4d062c1c334d8c2 and manufactured by INSTITUT VIRIONSERION GMBH. The authorized representative in Taiwan is UNISYS BIOMEDICAL CO..
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