Taiwan FDA registration 5df3617d02162b38cd24c7417c57138e
“B. Braun” Prontosan Wound Gel X
TW: “柏朗”博坦舒傷口凝膠
Taiwan·Risk Class 2·MD·B. BRAUN MEDICAL AG·Registered Jan 19, 2018 – Jan 19, 2023ExpiredRegistration details
- Analysis ID
- 5df3617d02162b38cd24c7417c57138e
- License Form
- Ministry of Health Medical Device Import No. 030833
- Customs Code
- DHA05603083305
Company information
- Manufacturer
- B. BRAUN MEDICAL AG
- Manufacturer Country
- Switzerland
- 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)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4022 Waterborne wound and burn coverings
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 19, 2018
- Expiry Date
- Jan 19, 2023
About this record
Access comprehensive regulatory information for “B. Braun” Prontosan Wound Gel X in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5df3617d02162b38cd24c7417c57138e and manufactured by B. BRAUN MEDICAL AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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