Taiwan FDA registration 6c79e21d51bd9c783f9714b5bb479e21
"Renver" multi-dense printing mold automatic mixer (unsterilized)
TW: “倫佛”多而密印模材自動混合機(未滅菌)
Taiwan·Risk Class 1·RENFERT GMBH·Registered May 04, 2007 – May 04, 2022CancelledRegistration details
- Analysis ID
- 6c79e21d51bd9c783f9714b5bb479e21
- Customs Code
- DHA04400582300
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 Dentistry
- Product Type (Level 2)
- F.3100 Dental and mercury appliances
- Import Information
- import
Dates and status
- Registration Date
- May 04, 2007
- Expiry Date
- May 04, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Renver" multi-dense printing mold automatic mixer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6c79e21d51bd9c783f9714b5bb479e21 and manufactured by RENFERT GMBH. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).
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