Pure Global

"Kobayashi" denture fixative (unsterilized) - Taiwan Registration c601dfd66f8442a44247217427eab9cd

Access comprehensive regulatory information for "Kobayashi" denture fixative (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c601dfd66f8442a44247217427eab9cd and manufactured by KOBAYASHI PHARMACEUTICAL CO., LTD.. The authorized representative in Taiwan is Xile Enterprises Limited.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
c601dfd66f8442a44247217427eab9cd
Registration Details
Taiwan FDA Registration: c601dfd66f8442a44247217427eab9cd
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Kobayashi" denture fixative (unsterilized)
TW: โ€œๅฐๆž—โ€ๅ‡็‰™ๅ›บๅฎšๅŠ‘๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

c601dfd66f8442a44247217427eab9cd

DHA04400615806

Company Information

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

import

Dates and Status

Sep 19, 2007

Sep 19, 2017

Nov 28, 2019

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ