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"Bayertin" bone replacement - Taiwan Registration 0c821c4b918fcaa8efbdcad37dbedc81

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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0c821c4b918fcaa8efbdcad37dbedc81
Registration Details
Taiwan FDA Registration: 0c821c4b918fcaa8efbdcad37dbedc81
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Device Details

"Bayertin" bone replacement
TW: โ€œๆ‹œ่€ณๅบญโ€้ชจๆ›ฟไปฃ็‰ฉ
Risk Class 2
Cancelled

Registration Details

0c821c4b918fcaa8efbdcad37dbedc81

DHA00602103002

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedics

N.3045 Absorbable Calcium Salt Bone Cavity Filling Device

import

Dates and Status

May 18, 2010

May 18, 2015

May 21, 2018

Cancellation Information

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