Taiwan FDA registration e682b780a381cadc51db3c5756c8e54e
"Bayer Janice" bridge system for bone explants
TW: “拜耳珍妮絲”骨內植體用牙橋系統
Taiwan·Risk Class 2·BIOGENESIS CO., LTD.·Registered Jun 13, 2012 – Jun 13, 2017CancelledRegistration details
- Analysis ID
- e682b780a381cadc51db3c5756c8e54e
- Customs Code
- DHA00602367302
Company information
- Manufacturer
- BIOGENESIS CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- DENMAX CORPORATION
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.3630 Bolsters for intraosseous implants
- Import Information
- import
Dates and status
- Registration Date
- Jun 13, 2012
- Expiry Date
- Jun 13, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bayer Janice" bridge system for bone explants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e682b780a381cadc51db3c5756c8e54e and manufactured by BIOGENESIS CO., LTD.. The authorized representative in Taiwan is DENMAX CORPORATION.
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