Taiwan FDA registration cd6f43c1f1aeaf076442e6ad04b640ef
Ankmeri bone plate
TW: 安克美骨板
Taiwan·Risk Class 3·BIOMATERIALS KOREA, INC.·Registered Feb 02, 2012 – Feb 02, 2017CancelledRegistration details
- Analysis ID
- cd6f43c1f1aeaf076442e6ad04b640ef
- Customs Code
- DHA00602324606
Company information
- Manufacturer
- BIOMATERIALS KOREA, INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- CONCERN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3640 Bone Implants
- Import Information
- import
Dates and status
- Registration Date
- Feb 02, 2012
- Expiry Date
- Feb 02, 2017
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Ankmeri bone plate in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number cd6f43c1f1aeaf076442e6ad04b640ef and manufactured by BIOMATERIALS KOREA, INC.. The authorized representative in Taiwan is CONCERN LTD..
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