Taiwan FDA registration 8635d5bdea741ffe1051ff4032175716
“ERBE” APCapplicator
TW: “艾柏”氬氣電漿凝固探頭
Taiwan·Risk Class 2·MD·ERBE ELEKTROMEDIZIN GMBH·Registered Dec 05, 2017 – Dec 05, 2027ActiveRegistration details
- Analysis ID
- 8635d5bdea741ffe1051ff4032175716
- License Form
- Ministry of Health Medical Device Import No. 030577
- Customs Code
- DHA05603057700
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 05, 2017
- Expiry Date
- Dec 05, 2027
About this record
Access comprehensive regulatory information for “ERBE” APCapplicator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8635d5bdea741ffe1051ff4032175716 and manufactured by ERBE ELEKTROMEDIZIN GMBH. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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