Taiwan FDA registration 0aefb57d3cdf512811b0707033e81972
"Baredon" denture adhesive (unsterilized)
TW: "百瑞登"假牙黏著劑(未滅菌)
Taiwan·Risk Class 1·BREDENT GMBH & CO. KG·Registered Oct 29, 2012 – Oct 29, 2017CancelledRegistration details
- Analysis ID
- 0aefb57d3cdf512811b0707033e81972
- Customs Code
- DHA04401231903
Company information
- Manufacturer
- BREDENT GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- Piloter International Trading Corp.
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
- Oct 29, 2012
- Expiry Date
- Oct 29, 2017
- Cancellation Date
- Dec 05, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Baredon" 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 0aefb57d3cdf512811b0707033e81972 and manufactured by BREDENT GMBH & CO. KG. The authorized representative in Taiwan is Piloter International Trading Corp..
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