Taiwan FDA registration cffaaec16da01a9de085fd63addd0120
“B.Braun” Xevonta High Flux & Low Flux dialyzer
TW: “柏朗”析望聚碸膜透析過濾器
Taiwan·Risk Class 2·MD·B. Braun Avitum Saxonia GmbH·Registered Feb 20, 2014 – Feb 20, 2029ActiveRegistration details
- Analysis ID
- cffaaec16da01a9de085fd63addd0120
- License Form
- Ministry of Health Medical Device Import No. 025786
- Customs Code
- DHA05602578602
Company information
- Manufacturer
- B. Braun Avitum Saxonia GmbH
- Manufacturer Country
- Germany
- 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)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5860 Highly permeable hemodialysis system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 20, 2014
- Expiry Date
- Feb 20, 2029
About this record
Access comprehensive regulatory information for “B.Braun” Xevonta High Flux & Low Flux dialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cffaaec16da01a9de085fd63addd0120 and manufactured by B. Braun Avitum Saxonia GmbH. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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