Taiwan FDA registration fb0214eb03ad16cfae6e4e9dae42a9c2
Teryleaf Sendo Denture Adhesive (Non-Sterile)
TW: 中美生醫 仙同假牙黏著劑 (未滅菌)
Taiwan·Risk Class 1·MD·NIPPON ZETTOC CO., LTD.·Registered Aug 05, 2020 – Aug 05, 2025ExpiredRegistration details
- Analysis ID
- fb0214eb03ad16cfae6e4e9dae42a9c2
- License Form
- Ministry of Health Medical Device Import No. 021829
- Customs Code
- DHA09402182907
Company information
- Manufacturer
- NIPPON ZETTOC CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- CHUNG MEI BIOPHARMA 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 Dental devices
- Product Type (Level 2)
- F3490 Sodium aminomethylcellulose, and/or polyethylene methyl ether sodium calcium, maleic acid compound salt denture adhesive
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 05, 2020
- Expiry Date
- Aug 05, 2025
About this record
Access comprehensive regulatory information for Teryleaf Sendo Denture Adhesive (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 fb0214eb03ad16cfae6e4e9dae42a9c2 and manufactured by NIPPON ZETTOC CO., LTD.. The authorized representative in Taiwan is CHUNG MEI BIOPHARMA CO., LTD..
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