Taiwan FDA registration 0c821c4b918fcaa8efbdcad37dbedc81

"Bayertin" bone replacement

TW: “拜耳庭”骨替代物

Taiwan·Risk Class 2·BIOMATLANTE·Registered May 18, 2010 – May 18, 2015Cancelled

Registration details

Analysis ID: 0c821c4b918fcaa8efbdcad37dbedc81
Customs Code: DHA00602103002

Company information

Manufacturer: BIOMATLANTE
Manufacturer Country: France
Authorized Representative: CHYA HUNG MEDICAL TREATMENT INSTRUMENTS FACTORY CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.3045 Absorbable Calcium Salt Bone Cavity Filling Device
Import Information: import

Dates and status

Registration Date: May 18, 2010
Expiry Date: May 18, 2015
Cancellation Date: May 21, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Bayertin" bone replacement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0c821c4b918fcaa8efbdcad37dbedc81 and manufactured by BIOMATLANTE. The authorized representative in Taiwan is CHYA HUNG MEDICAL TREATMENT INSTRUMENTS FACTORY CO., LTD..

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