Taiwan FDA registration dc4b21ea30ce1230fa9a249253f35961
“BOWA” ERGO 315R
TW: “博華”亞克歐血管閉合器械
Taiwan·Risk Class 2·MD·BOWA-ELECTRONIC GMBH & CO. KG·Registered Feb 13, 2023 – Feb 13, 2028ActiveRegistration details
- Analysis ID
- dc4b21ea30ce1230fa9a249253f35961
- License Form
- Ministry of Health Medical Device Import No. 036410
- Customs Code
- DHA05603641007
Company information
- Manufacturer
- BOWA-ELECTRONIC GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- SMARTECH MEDICAL 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
- Feb 13, 2023
- Expiry Date
- Feb 13, 2028
About this record
Access comprehensive regulatory information for “BOWA” ERGO 315R in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc4b21ea30ce1230fa9a249253f35961 and manufactured by BOWA-ELECTRONIC GMBH & CO. KG. The authorized representative in Taiwan is SMARTECH MEDICAL CO., LTD..
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