Taiwan FDA registration d51a938b6d830e50be014639b325ef96
“B.Braun” Celsite Implantable vascular access systems
TW: “柏朗” 紓賽植入型血管注射系統
Taiwan·Risk Class 2·MD·B.Braun Medical·Registered Oct 11, 2013 – Oct 11, 2028ActiveRegistration details
- Analysis ID
- d51a938b6d830e50be014639b325ef96
- License Form
- Ministry of Health Medical Device Import No. 025367
- Customs Code
- DHA05602536708
Company information
- Manufacturer
- B.Braun Medical
- Manufacturer Country
- France
- Authorized Representative
- B. BRAUN TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5965 Subcutaneous implantable intravascular injection port and catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 11, 2013
- Expiry Date
- Oct 11, 2028
About this record
Access comprehensive regulatory information for “B.Braun” Celsite Implantable vascular access systems in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d51a938b6d830e50be014639b325ef96 and manufactured by B.Braun Medical. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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