Taiwan FDA registration 924dafce4ff2cbda7f2264d6eb5ef92b
"Fresh Vision" denture adhesive (unsterilized)
TW: "新鮮視"假牙黏著劑(未滅菌)
Taiwan·Risk Class 1·BONYF AG·Registered Apr 03, 2012 – Apr 03, 2017CancelledRegistration details
- Analysis ID
- 924dafce4ff2cbda7f2264d6eb5ef92b
- Customs Code
- DHA04401155701
Company information
- Manufacturer
- BONYF AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- DAPHA TRADING CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification range of medical equipment management measures "sodium amino methylcellulose, and/or polyethylene methyl ether calcium sodium maleic acid compound salt denture adhesive (F.3490)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3490 Aminomethyl fiber-vigan metal, and/or polyethylene methyl ether butylate calcium butylate calcium compound denture adhesive
- Import Information
- import
Dates and status
- Registration Date
- Apr 03, 2012
- Expiry Date
- Apr 03, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Fresh Vision" denture adhesive (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 924dafce4ff2cbda7f2264d6eb5ef92b and manufactured by BONYF AG. The authorized representative in Taiwan is DAPHA TRADING CO., LTD..
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