Taiwan FDA registration 0e3111117356dedd8ebb571414f74d84
“B. Braun” Aesculap Electrosurgical System
TW: “柏朗”雅氏雙極電燒系統
Taiwan·Risk Class 2·MD·AESCULAP AG·Registered Jun 29, 2022 – Jun 29, 2027ActiveRegistration details
- Analysis ID
- 0e3111117356dedd8ebb571414f74d84
- License Form
- Ministry of Health Medical Device Import No. 035588
- Customs Code
- DHA05603558804
Company information
- Manufacturer
- AESCULAP AG
- Manufacturer Country
- Germany
- Authorized Representative
- B. BRAUN TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 29, 2022
- Expiry Date
- Jun 29, 2027
About this record
Access comprehensive regulatory information for “B. Braun” Aesculap Electrosurgical System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0e3111117356dedd8ebb571414f74d84 and manufactured by AESCULAP AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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