Taiwan FDA registration 25b7ccc5f10a481607eae3ffd2bcc198
“Adeor” HiCUT High Speed Instrument
TW: “安迪爾”海戈高速切割器械工具
Taiwan·Risk Class 2·MD·ADEOR MEDICAL AG·Registered Jun 16, 2023 – Jun 16, 2028ActiveRegistration details
- Analysis ID
- 25b7ccc5f10a481607eae3ffd2bcc198
- License Form
- Ministry of Health Medical Device Import No. 036543
- Customs Code
- DHA05603654300
Company information
- Manufacturer
- ADEOR MEDICAL AG
- Manufacturer Country
- Germany
- Authorized Representative
- CHAWEI CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G4680 Bronchoscope (soft or rigid) and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 16, 2023
- Expiry Date
- Jun 16, 2028
About this record
Access comprehensive regulatory information for “Adeor” HiCUT High Speed Instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25b7ccc5f10a481607eae3ffd2bcc198 and manufactured by ADEOR MEDICAL AG. The authorized representative in Taiwan is CHAWEI 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