2,582 results · 59ms · Sources: EU EUDAMED, US FDA

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MEDLINE'S EXAMIN, OPERATING ROOM/SURG LIGHTS/LAMPS

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

SW OPERATING LAMPS

FDA Adverse Event
Malfunction ·MAQUET SAS·Product code FXR·November 28, 2019

3611 LITE GLOVE

FDA Adverse Event
Malfunction ·COVIDIEN·Product code LYU·September 27, 2016

ST. FRANCIS OPERATING THEATRE LAMP, MODELS OLH01-125 AND LC-055

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ATELLICA CH 930 ANALYZER

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·July 22, 2024

HARMONY DUAL LA500 SURGICAL LIGHT

FDA Adverse Event
STERIS CORPORATION - MONTGOMERY·Product code FQO·November 6, 2014

DIMENSION EXL WITH LM

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·February 29, 2024

DIMENSION EXL 200

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·August 16, 2016

ATELLICA CH 930 ANALYZER

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·May 11, 2021

COBAS INTEGRA 400 PLUS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 13, 2013

COBAS INTEGRA 400 PLUS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 15, 2013

SUNNEX INC.

FDA Adverse Event
Malfunction ·SUNNEX INC.·Product code KZF·October 22, 2008

COBAS INTEGRA 800

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·December 15, 2010

MLX 300W XENON LIGHTSOURCE

FDA Adverse Event
Malfunction ·INTEGRA YORK, PA INC.·Product code FCW·October 11, 2016

HARMONY LC SURGICAL LIGHT

FDA Adverse Event
STERIS CORPORATION - MONTGOMERY·Product code FTD·January 26, 2011

VIDEO SYSTEM

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·November 17, 2020

OPMI VARIO / FLOOR STAND S88

FDA Adverse Event
Injury ·CARL ZEISS MEDITEC AG·Product code EPT·January 9, 2014

VISERA ELITE XENON LIGHT SOURCE

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code NWB·September 1, 2021

ARCHITECT C8000 SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·June 7, 2010

EVIS EXERA III XENON LIGHT SOURCE

FDA Adverse Event
Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code NWB·March 24, 2023