Pure Global

Fijaos bone cutting instrument - Taiwan Registration 99e819a7995e753ea63339378442ce46

Access comprehensive regulatory information for Fijaos bone cutting instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 99e819a7995e753ea63339378442ce46 and manufactured by FRIADENT GMBH. The authorized representative in Taiwan is Taiwan Branch of American Denspie 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
99e819a7995e753ea63339378442ce46
Registration Details
Taiwan FDA Registration: 99e819a7995e753ea63339378442ce46
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Fijaos bone cutting instrument
TW: ้ฃ›้›…ๆญๆ–ฏๅˆ‡้ชจๅ™จๆขฐ
Risk Class 2
Cancelled

Registration Details

99e819a7995e753ea63339378442ce46

DHA00601699201

Company Information

Germany

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

Aug 14, 2006

Aug 14, 2011

Nov 06, 2012

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ