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Recordon denture adhesive (unsterilized) - Taiwan Registration 2ea2a55a6ad9bb1f5a17de1603252871

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..

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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2ea2a55a6ad9bb1f5a17de1603252871
Registration Details
Taiwan FDA Registration: 2ea2a55a6ad9bb1f5a17de1603252871
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Device Details

Recordon denture adhesive (unsterilized)
TW: ็‘žๅฏ็™ปๅ‡็‰™้ป่‘—ๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

2ea2a55a6ad9bb1f5a17de1603252871

Company Information

Taiwan, Province of China

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 Dentistry

F.3490 Aminomethyl fiber-vigan metal, and/or polyethylene methyl ether butylate calcium butylate calcium compound denture adhesive

Domestic

Dates and Status

Sep 02, 2013

Sep 02, 2023

Sep 25, 2019

Cancellation Information

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