Taiwan FDA registration 1e23439ed943bb1f4a7ba6791e170070

"Fettden" denture liner (unsterilized)

TW: “飛特登”假牙襯墊 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·FITTYDENT INTERNATIONAL GMBH·Registered May 30, 2007 – May 30, 2022Cancelled
Registration details
Analysis ID
1e23439ed943bb1f4a7ba6791e170070
Customs Code
DHA04400592008
Company information
Manufacturer Country
Austria
Authorized Representative
HORIZON INSTRUMENTS CO. ,LTD.
Product details
Intended Use
Limited to the first level recognition range of denture liners (F.3540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1)
F Dentistry
Product Type (Level 2)
F.3540 No prescription denture pad required
Import Information
import
Dates and status
Registration Date
May 30, 2007
Expiry Date
May 30, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Fettden" denture liner (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1e23439ed943bb1f4a7ba6791e170070 and manufactured by FITTYDENT INTERNATIONAL GMBH. The authorized representative in Taiwan is HORIZON INSTRUMENTS 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.

Free DatabasePowered by Pure Global AI89,000+ Devices