25 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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AirFit N20
FDA 510(k)
FDA Class 2
·Anesthesiology
LuxaPrint Ortho Plus 405
FDA UDI
DMG Chemisch-Pharmazeutische Fabrik GmbH·EDMG1712120·(Meth) acrylate-based light-curing resin exclus...
LuxaPrint Ortho Plus 405
FDA UDI
DMG Digital Enterprises SE·D9821712120·(Meth) acrylate-based light-curing resin exclus...
Key Surgical K-Wires and Steinmann Pins
FDA UDI
KEY SURGICAL, INC.·00849771012795·K-Wires, Double diamond, .045-inch (1.1mm) diam...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293043·
NA
FDA UDI
KEY SURGICAL, INC.·10849771049415·K-Wires, Double diamond, .045-inch (1.1mm) diam...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484559·K-Wire w. double end lanzet point _x000D_...
K-Wire w. double end lanzet point 1.1mm/229mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM712120·K-Wire w. double end lanzet point
1.1mm/...
Sklar®
FDA UDI
SKLAR CORPORATION·10649111388699·MICRO MOSQ FCP CVD SERR 4"
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383552639·Gutta Percha Points is used to root canal filin...
Life Instruments
FDA UDI
Life Instrument Corporation·M9307171212310·#2 Ring Curette lateral
Life Instruments
FDA UDI
Life Instrument Corporation·M9307171212010·#2 Ring Curette straight
MEDTRONIC CONTOUR 3D ANNULOPLASTY RING, MODEL 690R
FDA 510(k)
FDA Class 2
·Cardiovascular
ESPRIT VENTILATOR SPEAKING MODE OPTION, MODEL V1000
FDA 510(k)
FDA Class 2
·Anesthesiology
HEARTMATE 3 VAD MODULAR CABLE
FDA Adverse Event
Malfunction
·THORATEC CORPORATION·Product code DSQ·February 10, 2023
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·June 14, 2013
COULTER HMX HEMATOLOGY ANALYZER WITH AUTOLOADER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·July 1, 2011
RESTORE ADVANCED RECHARGEABLE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 22, 2008
PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·October 20, 2025
PLASTIPAK LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·October 20, 2025