Taiwan FDA registration 8d9fbef5cce71165712d4bbae14a1d35
“ERBE” Bipolar Forceps
TW: “艾柏”雙極電燒鑷子
Taiwan·Risk Class 2·MD·ERBE ELEKTROMEDIZIN GMBH·Registered Dec 12, 2018 – Dec 12, 2028ActiveRegistration details
- Analysis ID
- 8d9fbef5cce71165712d4bbae14a1d35
- License Form
- Ministry of Health Medical Device Import No. 031923
- Customs Code
- DHA05603192301
Company information
- Manufacturer
- ERBE ELEKTROMEDIZIN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ERA BIOTEQ ENTERPRISE 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)
- I4400 Electric knife for cutting and hemostasis and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 12, 2018
- Expiry Date
- Dec 12, 2028
About this record
Access comprehensive regulatory information for “ERBE” Bipolar Forceps in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8d9fbef5cce71165712d4bbae14a1d35 and manufactured by ERBE ELEKTROMEDIZIN GMBH. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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