Taiwan FDA registration 25a8d8a557ed5f174eed78686c5f4cc4
“ERBE” FiAPC probe
TW: “艾柏”氬氣離子凝結用探頭
Taiwan·Risk Class 2·MD·ERBE ELEKTROMEDIZIN GMBH·Registered Dec 02, 2012 – Dec 02, 2027ActiveRegistration details
- Analysis ID
- 25a8d8a557ed5f174eed78686c5f4cc4
- License Form
- Department of Health Medical Device Import No. 024212
- Customs Code
- DHA00602421207
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 02, 2012
- Expiry Date
- Dec 02, 2027
About this record
Access comprehensive regulatory information for “ERBE” FiAPC probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25a8d8a557ed5f174eed78686c5f4cc4 and manufactured by ERBE ELEKTROMEDIZIN GMBH. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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