Taiwan FDA registration 3ac2677a2f7410a72453f4ae6198e0f4

"Bayer Janice" tooth intraosseous implant attachment (unsterilized)　

TW: “拜耳珍妮絲”牙齒骨內植入物附件 (未滅菌)　

Taiwan·Risk Class 1·BIOGENESIS CO., LTD.·Registered May 12, 2011 – May 12, 2016Cancelled

Registration details

Analysis ID: 3ac2677a2f7410a72453f4ae6198e0f4
Customs Code: DHA04401034507

Company information

Manufacturer: BIOGENESIS CO., LTD.
Manufacturer Country: Korea, Republic of
Authorized Representative: DENMAX CORPORATION

Product details

Intended Use: Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.3980 Intradental implant manipulation equipment
Import Information: import

Dates and status

Registration Date: May 12, 2011
Expiry Date: May 12, 2016
Cancellation Date: Aug 21, 2018

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Bayer Janice" tooth intraosseous implant attachment (unsterilized)　 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3ac2677a2f7410a72453f4ae6198e0f4 and manufactured by BIOGENESIS CO., LTD.. The authorized representative in Taiwan is DENMAX CORPORATION.

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