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

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COULTER ACT 5DIFF AL HEMATOLOGY ANALYZER

FDA 510(k)
FDA Class 2 ·Hematology

Medial Pilon Plate, Right, Short, 13-Hole

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665024661·

Battalion

FDA UDI
ALPHATEC SPINE, INC.·00840967187488·Battalion, LLIF Trial, 15°, 20 mm Wide, 13 mm X...

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0120130·Screwdriver, Polyaxial, Standard, Fixed Tap Sle...

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710620320130·Quad Channel Met-Traverse, 32mm x 13mm

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710810320130·Dwyer Calcaneal Guide, 32mm x 13mm

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710820320130·Zadik Calcaneal Guide, 32mm x 13°

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710450320130·Medial Guide, Closing Wedge Osteotomy, 32mm x 13mm

OMNIPORT

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

LIFESOURCE MODELS UA-787, UA 787PC, UA-787T

FDA 510(k)
FDA Class 2 ·Cardiovascular

SPECTRA WAVEWRITER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 20, 2019

SCP PANEL CENTRIFUGE JMS

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·November 5, 2013

SCP PANEL CENTRIFUGE JMS

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·March 14, 2014

SCP CONTROL PANEL

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012

CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

FDA Adverse Event
Malfunction ·LIVANOVA DEUTSCHLAND·Product code DWA·January 19, 2018

CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

FDA Adverse Event
Malfunction ·LIVANOVA DEUTSCHLAND GMBH·Product code DWA·January 5, 2022

STOCKERT JMS CENTRIFUGAL PUMP SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012

EON MINI

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

COLLEAGUE TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·March 28, 2011

ORTHO PROVUE

FDA Adverse Event
Malfunction ·MICRO TYPING SYSTEMS, INC.·Product code KSZ·April 21, 2008