Taiwan FDA registration 60d3c8d19258d17612acb2757087f860
“ERBE”HybridAPC Probe
TW: “艾柏”氬氣海博刀探針
Taiwan·Risk Class 2·MD·ERBE ELEKTROMEDIZIN GMBH·Registered Aug 04, 2017 – Aug 04, 2027ActiveRegistration details
- Analysis ID
- 60d3c8d19258d17612acb2757087f860
- License Form
- Ministry of Health Medical Device Import No. 030049
- Customs Code
- DHA05603004901
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 orthopedic surgical devices;; H Gastroenterology-urology devices
- Product Type (Level 2)
- H4300 Endoscope electric knife and accessories;; I4400 Electrosurgical Knife for Cutting and Hemostasis and Accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 04, 2017
- Expiry Date
- Aug 04, 2027
About this record
Access comprehensive regulatory information for “ERBE”HybridAPC Probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60d3c8d19258d17612acb2757087f860 and manufactured by ERBE ELEKTROMEDIZIN GMBH. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
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