Taiwan FDA registration 2146a105abac4f83de96ea9ad96e492f
“BOWA” ERGO 310D Laparoscope vessel sealer
TW: “博華”亞克歐腹腔鏡血管閉合器械
Taiwan·Risk Class 2·MD·BOWA-ELECTRONIC GMBH & CO. KG·Registered Feb 03, 2017 – Feb 03, 2027ActiveRegistration details
- Analysis ID
- 2146a105abac4f83de96ea9ad96e492f
- License Form
- Ministry of Health Medical Device Import No. 029358
- Customs Code
- DHA05602935801
Company information
- Manufacturer
- BOWA-ELECTRONIC GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- SMARTECH MEDICAL 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
- Feb 03, 2017
- Expiry Date
- Feb 03, 2027
About this record
Access comprehensive regulatory information for “BOWA” ERGO 310D Laparoscope vessel sealer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2146a105abac4f83de96ea9ad96e492f and manufactured by BOWA-ELECTRONIC GMBH & CO. KG. The authorized representative in Taiwan is SMARTECH MEDICAL CO., LTD..
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