Taiwan FDA registration 80049c3e0640542191c7983b86afdfcb
“Renfert” Capsule Mixer (Non-Sterile)
TW: “倫芙” 牙科用膠囊混合器 (未滅菌)
Taiwan·Risk Class 1·MD·RENFERT GMBH·Registered Apr 20, 2021 – Apr 20, 2026ExpiredRegistration details
- Analysis ID
- 80049c3e0640542191c7983b86afdfcb
- License Form
- Ministry of Health Medical Device Import No. 022492
- Customs Code
- DHA09402249203
Company information
- Manufacturer
- RENFERT GMBH
- Manufacturer Country
- Germany
- 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 “Renfert” 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 80049c3e0640542191c7983b86afdfcb and manufactured by RENFERT GMBH. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).
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