Taiwan FDA registration c14c5c9f58b2a96697255427c4fd8147

"Quies" Putes denture adhesive (unsterilized)

TW: “魁士”普特斯假牙黏著劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·QUEISSER PHARMA GMBH & CO., KG·Registered Dec 05, 2007 – Dec 05, 2012Cancelled
Registration details
Analysis ID
c14c5c9f58b2a96697255427c4fd8147
Customs Code
DHA04400636001
Company information
Manufacturer Country
Germany
Authorized Representative
Ruth Enterprises
Product details
Intended Use
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)".
Product Type (Level 1)
F Dentistry
Product Type (Level 2)
F.3490 Aminomethyl fiber-vigan metal, and/or polyethylene methyl ether butylate calcium butylate calcium compound denture adhesive
Import Information
import
Dates and status
Registration Date
Dec 05, 2007
Expiry Date
Dec 05, 2012
Cancellation Date
Apr 14, 2014
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Quies" Putes 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 c14c5c9f58b2a96697255427c4fd8147 and manufactured by QUEISSER PHARMA GMBH & CO., KG. The authorized representative in Taiwan is Ruth Enterprises.

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 DatabasePowered by Pure Global AI89,000+ Devices