Taiwan FDA registration 038bc2bc30b13a04221c589729b743e7
“OBS” Anchorage Screw
TW: “歐必適”牙科矯正釘
Taiwan·Risk Class 3·MD·BOMEI CO., LTD.·Registered Aug 25, 2021 – Feb 07, 2028ActiveRegistration details
- Analysis ID
- 038bc2bc30b13a04221c589729b743e7
- License Form
- Ministry of Health Medical Device Manufacturing No. 007178
Company information
- Manufacturer
- BOMEI CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BOMEI CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3640 Bone explants
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 25, 2021
- Expiry Date
- Feb 07, 2028
About this record
Access comprehensive regulatory information for “OBS” Anchorage Screw in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 038bc2bc30b13a04221c589729b743e7 and manufactured by BOMEI CO., LTD.. The authorized representative in Taiwan is BOMEI 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