Taiwan FDA registration 57fda29ee698c0b8281fd5225a30ea83
"Bayer Janice" bone explant system
TW: “拜耳珍妮絲”骨內植體系統
Taiwan·Risk Class 3·BIOGENESIS CO., LTD.·Registered Jul 19, 2012 – Jul 19, 2017CancelledRegistration details
- Analysis ID
- 57fda29ee698c0b8281fd5225a30ea83
- Customs Code
- DHA00602371502
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.3640 Bone Implants
- Import Information
- import
Dates and status
- Registration Date
- Jul 19, 2012
- Expiry Date
- Jul 19, 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" bone explant system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 57fda29ee698c0b8281fd5225a30ea83 and manufactured by BIOGENESIS CO., LTD.. The authorized representative in Taiwan is DENMAX CORPORATION.
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