72 results · 33ms · Sources: EU EUDAMED, US FDA

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LUMENIS VERSACUT TISSUE MORCELLATOR SYSTEM

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

VISIONARY 2000

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

CONVERGENCE CERVICAL SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·October 6, 2011

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 13, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·July 13, 2017

VPV SYSTEM

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF MEDOS·Product code JXG·January 6, 2014

CODMAN VIPV SYSTEM

FDA Adverse Event
Malfunction ·CODMAN & SHURTLEFF, INC. MEDOS S.A.·Product code JXG·November 5, 2010

CODMAN VPV SYSTEM

FDA Adverse Event
Malfunction ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·January 11, 2018

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·November 28, 2011

CODMAN VPV SYSTEM

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·October 1, 2016

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·January 7, 2016

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·June 29, 2012

CODMAN VPV SYSTEM

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·November 12, 2015

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·April 3, 2012

CODMAN VPV SYSTEM

FDA Adverse Event
Malfunction ·CODMAN & SHURTLEFF, INC, MEDOS S.A.·Product code JXG·October 11, 2010

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·December 15, 2016

CODMAN VPV SYSTEM

FDA Adverse Event
Malfunction ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·August 16, 2017

CODMAN VPV SYSTEM

FDA Adverse Event
Malfunction ·CODMAN & SHURTLEFF·Product code JXG·January 28, 2015

HS III PROXIMAL SEAL SYSTEM 3.8MM

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·March 14, 2013