Taiwan FDA registration 12a3517b9ba870d00540fc29d3d97ab6
"Yaman Gilbach" formed metal denture bed (unsterilized)
TW: "亞曼吉爾巴赫"成形金屬假牙床(未滅菌)
Taiwan·Risk Class 1·AMANN GIRRBACH AG·Registered May 15, 2013 – May 15, 2018CancelledRegistration details
- Analysis ID
- 12a3517b9ba870d00540fc29d3d97ab6
- Customs Code
- DHA04401302007
Company information
- Manufacturer
- AMANN GIRRBACH AG
- Manufacturer Country
- Austria
- Authorized Representative
- WINDENT ENTERPRISE CO., LTD.
Product details
- Intended Use
- It is limited to the first level of identification of the medical device management measures "Formed Metal Denture Bed (F3580)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3580 成型金屬假牙床
- Import Information
- import
Dates and status
- Registration Date
- May 15, 2013
- Expiry Date
- May 15, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Yaman Gilbach" formed metal denture bed (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 12a3517b9ba870d00540fc29d3d97ab6 and manufactured by AMANN GIRRBACH AG. The authorized representative in Taiwan is WINDENT ENTERPRISE 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