434 results · 29ms · Sources: EU EUDAMED, US FDA

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BIONET BM3PLUS PATIENT MONITOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

Integra® Miltex®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780169406·Integra® Miltex® Cassette, Slimline 7, Long, 8"...

Malecot

FDA UDI
COOK INCORPORATED·00827002148277·Percutaneous Malecot Nephrostomy Set

FIBONACCI™ PROXIMAL LATERAL TIBIA PLATE, RIGHT, 8 HOLE

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665035261·

OsteoMed

FDA UDI
OSTEOMED LLC·00845694038829·2.0mm x 8mm Midface Screw

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0840080·Distractor, Screw to Screw

K032008

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code LJT·May 31, 2007

SURGICAL DYNAMICS SPINAL RETRACTOR

FDA 510(k)
FDA Class 2 ·Orthopedic

STS RANGE , MODELS STS20,STS30,STS40

FDA 510(k)
FDA Class 2 ·Cardiovascular

ACRYSOF TORIC

FDA Adverse Event
Other ·ALCON RESEARCH, LTD/HUNTINGTON·Product code MJP·October 24, 2008

ACRYSOF RESTOR

FDA Adverse Event
Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·June 6, 2008

ENDO STICH SHORT INSTRUMENT

FDA Adverse Event
Injury ·NORTH HAVEN - USS·Product code MFJ·May 8, 2008

DONJOY PAIN BUSTER

FDA Adverse Event
Malfunction ·DONJOY DJO, LLC·Product code MEB·February 8, 2008

EASY AIR

FDA Adverse Event
Death ·PRECISION MEDICAL INC.·Product code BTI·October 7, 2010

ULTRACISION HARMONIC SCALPEL CURVED SHEARS (LCS) PISTOL GRIP 36CM - 15MM ACTIVE

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GEI·December 8, 2008

LIGAMAX-5MM ENDO CLIP APPLIER

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code FZP·July 24, 2008

EEA XL 25MM STAPLER WITH 3.5MM STAPLES

FDA Adverse Event
Injury ·NORTH HAVEN - USS·Product code GDW·September 8, 2008

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 29, 2013

TRUFILL DCS ORBIT DETACHABLE COILS COMPLEX

FDA Adverse Event
Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code HCG·May 9, 2011

ACCU-CHEK SPIRIT

FDA Adverse Event
Malfunction ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code LZG·July 23, 2008