Taiwan FDA registration cc753b742063e5486026a83d40b44b0a
“ERBE” BiClamp knife 220 Vessel sealing instrument
TW: “愛爾博”拋棄式百克鉗
Taiwan·Risk Class 2·MD·ERBE ELEKTROMEDIZIN GMBH·Registered Nov 24, 2022 – Nov 24, 2027ActiveRegistration details
- Analysis ID
- cc753b742063e5486026a83d40b44b0a
- License Form
- Ministry of Health Medical Device Import No. 036106
- Customs Code
- DHA05603610604
Company information
- Manufacturer
- ERBE ELEKTROMEDIZIN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ERA BIOTEQ ENTERPRISE 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
- Nov 24, 2022
- Expiry Date
- Nov 24, 2027
About this record
Access comprehensive regulatory information for “ERBE” BiClamp knife 220 Vessel sealing instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc753b742063e5486026a83d40b44b0a and manufactured by ERBE ELEKTROMEDIZIN GMBH. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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