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Sendo Denture Adhesive (Non-Sterile) - Taiwan Registration 23628348072873a1d0a4b57be142ddb6

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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23628348072873a1d0a4b57be142ddb6
Registration Details
Taiwan FDA Registration: 23628348072873a1d0a4b57be142ddb6
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Device Details

Sendo Denture Adhesive (Non-Sterile)
TW: ไป™ๅŒ ๅ‡็‰™้ป่‘—ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

23628348072873a1d0a4b57be142ddb6

Ministry of Health Medical Device Import No. 016123

DHA09401612302

Company Information

Japan

Product Details

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)".

F Dental devices

F3490 Sodium aminomethylcellulose, and/or polyethylene methyl ether sodium calcium, maleic acid compound salt denture adhesive

Imported from abroad

Dates and Status

Jan 28, 2016

Jan 28, 2021

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