Taiwan FDA registration 8f516f1198b96ab9119a05270fb05b6f
“ERBE” LAP Bisect
TW: “艾柏”腹鏡下百克剪
Taiwan·Risk Class 2·MD·ERBE ELEKTROMEDIZIN GMBH·Registered May 31, 2012 – May 31, 2027ActiveRegistration details
- Analysis ID
- 8f516f1198b96ab9119a05270fb05b6f
- License Form
- Department of Health Medical Device Import No. 023608
- Customs Code
- DHA00602360801
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
- May 31, 2012
- Expiry Date
- May 31, 2027
About this record
Access comprehensive regulatory information for “ERBE” LAP Bisect in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f516f1198b96ab9119a05270fb05b6f and manufactured by ERBE ELEKTROMEDIZIN GMBH. The authorized representative in Taiwan is ERA BIOTEQ ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices