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"Teryleaf" Sendo Denture Adhesive (Non-Sterile) - Taiwan Registration 49b74e979e65dc0817a068fa99cebe7f

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 49b74e979e65dc0817a068fa99cebe7f and manufactured by NIPPON ZETTOC CO., LTD.. The authorized representative in Taiwan is CHUNG MEI BIOPHARMA CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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49b74e979e65dc0817a068fa99cebe7f
Registration Details
Taiwan FDA Registration: 49b74e979e65dc0817a068fa99cebe7f
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Device Details

"Teryleaf" Sendo Denture Adhesive (Non-Sterile)
TW: "ไธญ็พŽ็”Ÿ้†ซ" ไป™ๅŒๅ‡็‰™้ป่‘—ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

49b74e979e65dc0817a068fa99cebe7f

Ministry of Health Medical Device Import No. 016603

DHA09401660300

Company Information

Japan

Product Details

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

Jun 01, 2016

Jun 01, 2021

Jun 15, 2023

Cancellation Information

Logged out

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