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Jedon Denture Adhesive Paste (Unsterilized) - Taiwan Registration 0120ac6438cf26c0ee7e1fa66b3cf83c

Access comprehensive regulatory information for Jedon Denture Adhesive Paste (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0120ac6438cf26c0ee7e1fa66b3cf83c and manufactured by QUEISSER PHARMA GMBH & CO., KG. The authorized representative in Taiwan is BEST OCEAN PHARMACEUTICAL 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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0120ac6438cf26c0ee7e1fa66b3cf83c
Registration Details
Taiwan FDA Registration: 0120ac6438cf26c0ee7e1fa66b3cf83c
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Device Details

Jedon Denture Adhesive Paste (Unsterilized)
TW: ๆฝ”็™ปไฟๆฝ”้ˆๅ‡็‰™้ป่‘—่†(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0120ac6438cf26c0ee7e1fa66b3cf83c

DHA04400134608

Company Information

Product Details

Dentures are applied to the base of the denture before being placed in the patient's mouth to increase the retention and comfort of the denture.

F Dentistry

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

import

Dates and Status

Oct 28, 2005

Oct 28, 2015

Aug 14, 2018

Cancellation Information

Logged out

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