Taiwan FDA registration e6d0b437cd772ff64e20df27fac3884c
"Pojin" capillary blood collection tube (unsterilized)
TW: “寶進” 毛細血液收集管(未滅菌)
Taiwan·Risk Class 1·VITREX MEDICAL A/S·Registered Mar 18, 2011 – Mar 18, 2016CancelledRegistration details
- Analysis ID
- e6d0b437cd772ff64e20df27fac3884c
- Customs Code
- DHA04401005409
Company information
- Manufacturer
- VITREX MEDICAL A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- FIRST BLOOD BIOTECH CORP.
Product details
- Intended Use
- Limited to the first level identification range of "Capillary Blood Collection Tube (B.6150)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.6150 Capillary Blood Collection Tubes
- Import Information
- import
Dates and status
- Registration Date
- Mar 18, 2011
- Expiry Date
- Mar 18, 2016
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pojin" capillary blood collection tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e6d0b437cd772ff64e20df27fac3884c and manufactured by VITREX MEDICAL A/S. The authorized representative in Taiwan is FIRST BLOOD BIOTECH CORP..
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