25 results · 30ms · Sources: EU EUDAMED, US FDA

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PHILLIPS OMNIDIAGNOST ELEVA

FDA 510(k)
FDA Class 2 ·Radiology

N.A.

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR20320461·BioTorque wires Straight-Arch-F. max. .018"x.025"

SlimLine®

FDA UDI
ZIMMER SPINE, INC.·00889024403604·

ihcDirect® p120 Ab, 15mL

FDA UDI
NOVODIAX, INC.·00850000596900·Clone R1013

ihcDirect® p120 Ab, 5mL

FDA UDI
NOVODIAX, INC.·00850000596894·Clone R1013

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710410320460·Anterior Closing Wedge Osteotomy Guide, 32mm x ...

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710420320460·Anterio Lateral Wedge Osteotomy Guide, 32mm x 46mm

MODIFICATION TO AUTOMATED NON-INVASIVE BLOOD PRESSURE MONITOR, MODEL BPM-100

FDA 510(k)
FDA Class 2 ·Cardiovascular

VITAL SCIENTIFIC COAGULATION CONTROL,COAGULATION CONTROL LEVEL 1,2,3,QUIKCOAG COAGULATION CONTROL

FDA 510(k)
FDA Class 2 ·Hematology

QUATTRODE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 26, 2013

ACCU-CHEK ® INFORM METER

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·March 28, 2011

STERIS SYSTEM 1

FDA Adverse Event
Other ·STERIS CORPORATION·Product code MLR·April 21, 2008

SYNCHRO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·April 8, 2010

SYNCHRO GUIDEWIRE

FDA Adverse Event
Death ·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·August 2, 2010

SYNCHRO GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·May 27, 2010

SYNCHRO GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - SALT LAKE CITY·Product code DQX·April 15, 2010

SYNCHRO-14 STRAIGHT 200-35CM

FDA Adverse Event
Malfunction ·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code DQX·December 12, 2023

SYNCHRO-10 STRAIGHT 200CM

FDA Adverse Event
Malfunction ·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code DQX·October 13, 2023

SYNCHRO-14 STRAIGHT 200-35CM

FDA Adverse Event
Malfunction ·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code DQX·November 13, 2023

TITANIUM (TI) RIB SLEEVE-SIZE 8 220MM RADIUS

FDA Adverse Event
Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code MDI·August 16, 2018