Taiwan FDA registration 2ea2a55a6ad9bb1f5a17de1603252871
Recordon denture adhesive (unsterilized)
TW: 瑞可登假牙黏著劑(未滅菌)
Registration details
- Analysis ID
- 2ea2a55a6ad9bb1f5a17de1603252871
Company information
- Manufacturer
- RECO-DENT INTERNATIONAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- RECO-DENT INTERNATIONAL 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
- Domestic
Dates and status
- Registration Date
- Sep 02, 2013
- Expiry Date
- Sep 02, 2023
- Cancellation Date
- Sep 25, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Recordon 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 2ea2a55a6ad9bb1f5a17de1603252871 and manufactured by RECO-DENT INTERNATIONAL CO., LTD.. The authorized representative in Taiwan is RECO-DENT INTERNATIONAL CO., LTD..
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