27 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SNAP MODEL 8 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
Innospire Deluxe
FDA UDI
VEGA TECHNOLOGIES INC.·06946159502061·1110064
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100540·Caddie, 8.5mm Screws
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100140·Implant Tray, Cosmolock, Arcamed
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K1100140·Implant Tray
BREDENT NOVO.LIGN A/ BREDENT NOVO.LIGN P
FDA 510(k)
FDA Class 2
·Dental
4C-ES CELL, MODELS 7547187, 7547188, 7547189, 7547190
FDA 510(k)
FDA Class 2
·Hematology
Trilogy®
FDA UDI
Zimmer, Inc.·00889024637160·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024360648·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024637153·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024637184·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024637177·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024360624·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024360655·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024360631·
EXPRESS BILIARY SD PREMOUNTED STENT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code FGE·August 30, 2006
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·May 13, 2013
JINRO¿ PIGTAIL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code FFA·June 1, 2011
GE OEC 9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·August 14, 2008
BD PLASTIPAK¿ - 3-PIECE SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·March 18, 2022