Taiwan FDA registration 577882efc181e9d6a5ce4b0a773f68ce
“SDI” Capsule Mixer (Non-Sterile)
TW: “思帝艾”牙科用膠囊混合器 (未滅菌)
Taiwan·Risk Class 1·MD·SDI LIMITED·Registered Apr 20, 2021 – Apr 20, 2026ExpiredRegistration details
- Analysis ID
- 577882efc181e9d6a5ce4b0a773f68ce
- License Form
- Ministry of Health Medical Device Import No. 022491
- Customs Code
- DHA09402249101
Company information
- Manufacturer
- SDI LIMITED
- Manufacturer Country
- Australia
- Authorized Representative
- DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.)
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
- Imported from abroad
Dates and status
- Registration Date
- Apr 20, 2021
- Expiry Date
- Apr 20, 2026
About this record
Access comprehensive regulatory information for “SDI” 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 577882efc181e9d6a5ce4b0a773f68ce and manufactured by SDI LIMITED. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).
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