Taiwan FDA registration 2fc7aa90363599b0b7617a0e93b5f035
"Denmei" prosthetic teeth base and surface (unsterilized)
TW: "登美" 人工牙的底和面 (未滅菌)
Registration details
- Analysis ID
- 2fc7aa90363599b0b7617a0e93b5f035
- Customs Code
- DHA04401299007
Company information
- Manufacturer
- DENMAT HOLDINGS, LLC.
- Manufacturer Country
- United States
- Authorized Representative
- AIREX CORP.
Product details
- Intended Use
- It is limited to the first level of identification scope of the medical device management method "bottom and surface of artificial teeth (F3910)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3910 Base and surface of artificial teeth
- Import Information
- import
Dates and status
- Registration Date
- May 08, 2013
- Expiry Date
- May 08, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Denmei" prosthetic teeth base and surface (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2fc7aa90363599b0b7617a0e93b5f035 and manufactured by DENMAT HOLDINGS, LLC.. The authorized representative in Taiwan is AIREX CORP..
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