Taiwan FDA registration dda12f5003212617a593fc94aea9d831
“Motion” Capsule Mixer (Non-Sterile)
TW: “茂生” 牙科用膠囊混合器 (未滅菌)
Taiwan·Risk Class 1·MD·MOTION DENTAL EQUIPMENT CORPORATION·Registered Aug 13, 2020 – Aug 13, 2025ExpiredRegistration details
- Analysis ID
- dda12f5003212617a593fc94aea9d831
- License Form
- Ministry of Health Medical Device Manufacturing No. 008514
Company information
- Manufacturer
- MOTION DENTAL EQUIPMENT CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MOTION DENTAL EQUIPMENT CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of dental and mercury instruments (F.3100) in the management of medical devices.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3100 Dental and mercury ware
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 13, 2020
- Expiry Date
- Aug 13, 2025
About this record
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.
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