Taiwan FDA registration 4a3dae94ced84660f6085932e406947a
"Frieton" R&F system equipment (unsterilized)
TW: “富瑞騰”富力歐系統器械（未滅菌）
Taiwan·Risk Class 1·FRIADENT GMBH·Registered Apr 03, 2006 – Apr 03, 2016CancelledRegistration details
- Analysis ID
- 4a3dae94ced84660f6085932e406947a
- Customs Code
- DHA04400341906
Company information
- Manufacturer
- FRIADENT GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Taiwan Branch of American Denspie Co., Ltd
Product details
- Intended Use
- Limited to the scope of first-class identification of medical equipment management methods (intradental implant attachments [F.3980]).
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3980 Intradental implant manipulation equipment
- Import Information
- import
Dates and status
- Registration Date
- Apr 03, 2006
- Expiry Date
- Apr 03, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Frieton" R&F system equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4a3dae94ced84660f6085932e406947a and manufactured by FRIADENT GMBH. The authorized representative in Taiwan is Taiwan Branch of American Denspie 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