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"Bone Lux" absorbs regenerative membranes - Taiwan Registration 434305213e8b8ab15ff01da57e17a2ea

Access comprehensive regulatory information for "Bone Lux" absorbs regenerative membranes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 434305213e8b8ab15ff01da57e17a2ea and manufactured by BOTISS BIOMATERIALS GMBH. The authorized representative in Taiwan is Straumann Group (Taiwan) Co. Ltd..

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434305213e8b8ab15ff01da57e17a2ea
Registration Details
Taiwan FDA Registration: 434305213e8b8ab15ff01da57e17a2ea
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Device Details

"Bone Lux" absorbs regenerative membranes
TW: โ€œ้ชจๅŠ›ๅฃซโ€ๅฏๅธๆ”ถๅ†็”Ÿ่†œ
Risk Class 2

Registration Details

434305213e8b8ab15ff01da57e17a2ea

DHA05603335602

Company Information

Germany

Product Details

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

F Dentistry

F.3930 Alveolar repair materials

import

Dates and Status

Feb 23, 2020

Feb 23, 2030