Taiwan FDA registration aab339265b4d98e0686e5cdbebc088f2

"Help you" denture adhesive (unsterilized)

TW: "幫您"假牙黏著劑(未滅菌)

Taiwan·Risk Class 1·BONYF AG·Registered Feb 22, 2011 – Feb 22, 2026Expired

Registration details

Analysis ID: aab339265b4d98e0686e5cdbebc088f2
Customs Code: DHA04400991305

Company information

Manufacturer: BONYF AG
Manufacturer Country: Switzerland
Authorized Representative: SUNDENT CORPORATION

Product details

Intended Use: It is limited to the first level of identification scope of the "Ethylene Oxide Polymer and/or Carboxymethyl Cellulose Sodium Denture Adhesive (F.3410)" of the Classification and Grading Management Measures for Medical Devices.
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.3410 Ethylene oxide polymer and/or carboxymethyl fibervetinol denture adhesive
Import Information: import

Dates and status

Registration Date: Feb 22, 2011
Expiry Date: Feb 22, 2026

About this record

Access comprehensive regulatory information for "Help you" 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 aab339265b4d98e0686e5cdbebc088f2 and manufactured by BONYF AG. The authorized representative in Taiwan is SUNDENT CORPORATION.

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.