Pure Global

“Mectron” Piezosurgery Bone Surgery Unit and Accessories - Taiwan Registration 3939ac5a8a218c6e8dd5e1f8c3e1a082

Access comprehensive regulatory information for “Mectron” Piezosurgery Bone Surgery Unit and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3939ac5a8a218c6e8dd5e1f8c3e1a082 and manufactured by MECTRON S.P.A.. The authorized representative in Taiwan is SUNDENT CORPORATION.

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
3939ac5a8a218c6e8dd5e1f8c3e1a082
Registration Details
Taiwan FDA Registration: 3939ac5a8a218c6e8dd5e1f8c3e1a082
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Mectron” Piezosurgery Bone Surgery Unit and Accessories
TW: “麥克龍”皮耶牙科超音波骨切割器及其配件
Risk Class 2
MD

Registration Details

3939ac5a8a218c6e8dd5e1f8c3e1a082

Ministry of Health Medical Device Import No. 029948

DHA05602994809

Company Information

Italy

Product Details

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

F Dental devices

F4120 bone cutters and accessories

Imported from abroad

Dates and Status

Jul 19, 2017

Jul 19, 2027