265 results · 22ms · Sources: EU EUDAMED, US FDA

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OTTO™ Disinfecting Cap

FDA 510(k)
FDA Class 2 ·General Hospital

OsteoMed

FDA UDI
OSTEOMED LLC·00845694018135·MFx 2.0mm x 6mm Angulated Locking Standard Screw

ceraMotion®

FDA UDI
DENTAURUM GmbH & Co.KG·J011252006400·ceraMotion® Me Opaque B1, 40 g / dental ceramic...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197059572·Varady micro phlebextractor 17.0cm

ceraMotion®

FDA UDI
DENTAURUM GmbH & Co.KG·J011252006200·ceraMotion® Me Opaque B1, 20 g / dental ceramic...

POWDER-FREE VINYL EXAM GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

Cogent Hemodynamic Monitoring System

FDA 510(k)
FDA Class 2 ·Cardiovascular

RX ACCULINK CAROTID STENT SYSTEM

FDA Adverse Event
Injury ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code NIM·April 28, 2006

PICC

FDA Adverse Event
Injury ·C.R. BARD, INC. (BASD)·Product code DQO·May 15, 2006

SABRE 2400 ESU

FDA Adverse Event
Malfunction ·CONMED ELECTROSURGERY·Product code GEI·July 25, 2006

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·November 8, 2006

INSERTER-MEDIUM

FDA Adverse Event
Malfunction ·SYNTHES TUTTLINGEN·Product code LXH·August 9, 2016

N595 PULSE OXIMETER

FDA Adverse Event
Malfunction ·NELLCOR PURITAN BENNETT, INC.·Product code DQA·June 12, 2006

ICL (IMPLANTABLE COLLAMER LENS)

FDA Adverse Event
Injury ·STAAR SURGICAL CO.·Product code HQL·March 20, 2006

VISION ICL IMPLANTABLE COLLAMER LENS

FDA Adverse Event
Injury ·STAAR SURGICAL·Product code HQL·June 30, 2006

MED-EL COMBI-40+ COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·June 9, 2006

KINMX PLUS, SML TIB B/PL ASSY

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS LIMERICK·Product code JWH·October 18, 2006

MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·May 2, 2006

MADEX PROTECTIV PLUS

FDA Adverse Event
Injury ·SMITHS MEDICAL M.D. INC.·Product code FOZ·October 10, 2006

RENU WITH MOISTURE LOC

FDA Adverse Event
Injury ·BASUCH & LOMB·Product code LPN·August 1, 2006