Taiwan FDA registration 3cd3db5fbfd466c49fdbd97b307e6e2a
"Schiffel" denture adhesive (unsterilized)
TW: "雪菲兒" 假牙黏著劑 (未滅菌)
Taiwan·Risk Class 1·SHEFFIELD PHARMACEUTICALS·Registered Jul 14, 2010 – Jul 14, 2025ExpiredRegistration details
- Analysis ID
- 3cd3db5fbfd466c49fdbd97b307e6e2a
- Customs Code
- DHA04400898601
Company information
- Manufacturer
- SHEFFIELD PHARMACEUTICALS
- Manufacturer Country
- United States
- Authorized Representative
- Xinmao Pharmaceutical Co., Ltd
Product details
- Intended Use
- Limited to the first level of identification scope of the "Sodium Amino Methyl Cellulose, and/or Polyethylene Methyl Ether Sodium Maleic Acid Calcium Sodium Compound Denture Adhesive (F.3490) for the Classification and Grading Management Measures for Medical Devices".
- 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
- Jul 14, 2010
- Expiry Date
- Jul 14, 2025
About this record
Access comprehensive regulatory information for "Schiffel" 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 3cd3db5fbfd466c49fdbd97b307e6e2a and manufactured by SHEFFIELD PHARMACEUTICALS. The authorized representative in Taiwan is Xinmao 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.
Free DatabasePowered by Pure Global AI89,000+ Devices