Taiwan FDA registration 23628348072873a1d0a4b57be142ddb6

Sendo Denture Adhesive (Non-Sterile)

TW: 仙同 假牙黏著劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·NIPPON ZETTOC CO., LTD.·Registered Jan 28, 2016 – Jan 28, 2021Expired
Registration details
Analysis ID
23628348072873a1d0a4b57be142ddb6
License Form
Ministry of Health Medical Device Import No. 016123
Customs Code
DHA09401612302
Company information
Manufacturer Country
Japan
Authorized Representative
SINO ADVANCE BIOTECH 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
Jan 28, 2016
Expiry Date
Jan 28, 2021
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About this record

Access comprehensive regulatory information for 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 23628348072873a1d0a4b57be142ddb6 and manufactured by NIPPON ZETTOC CO., LTD.. The authorized representative in Taiwan is SINO ADVANCE BIOTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NIPPON ZETTOC CO., LTD., and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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