Pure Global

“Motion” Capsule Mixer (Non-Sterile) - Taiwan Registration dda12f5003212617a593fc94aea9d831

Access comprehensive regulatory information for “Motion” Capsule Mixer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dda12f5003212617a593fc94aea9d831 and manufactured by MOTION DENTAL EQUIPMENT CORPORATION. The authorized representative in Taiwan is MOTION DENTAL EQUIPMENT 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
dda12f5003212617a593fc94aea9d831
Registration Details
Taiwan FDA Registration: dda12f5003212617a593fc94aea9d831
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Motion” Capsule Mixer (Non-Sterile)
TW: “茂生” 牙科用膠囊混合器 (未滅菌)
Risk Class 1
MD

Registration Details

dda12f5003212617a593fc94aea9d831

Ministry of Health Medical Device Manufacturing No. 008514

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of dental and mercury instruments (F.3100) in the management of medical devices.

F Dental devices

F3100 Dental and mercury ware

Produced in Taiwan, China

Dates and Status

Aug 13, 2020

Aug 13, 2025