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Biosonic bone cutter - Taiwan Registration 775affb449221ae084bab965e1bba7ba

Access comprehensive regulatory information for Biosonic bone cutter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 775affb449221ae084bab965e1bba7ba and manufactured by SATELEC, A COMPANY OF ACTEON GROUP. The authorized representative in Taiwan is FABRO INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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775affb449221ae084bab965e1bba7ba
Registration Details
Taiwan FDA Registration: 775affb449221ae084bab965e1bba7ba
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Device Details

Biosonic bone cutter
TW: ๅฟ…้ฉ้€š่ถ…้Ÿณๆณข้ชจๅˆ‡ๅ‰ฒๅ™จ
Risk Class 2
Cancelled

Registration Details

775affb449221ae084bab965e1bba7ba

DHA00602503006

Company Information

Product Details

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

F Dentistry

F.4120 Bone cutters and accessories thereof

import

Dates and Status

May 16, 2013

May 16, 2018

Apr 12, 2024

Cancellation Information

Logged out

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