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

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CONTACT DETACH

FDA 510(k)
FDA Class 2 ·General Hospital

Bone Conductor (BC-2)

FDA UDI
Natus Medical Denmark ApS·05713315009969·BC-2 Bone Conductor With Headband

JEDMED

FDA UDI
JEDMED INSTRUMENT COMPANY·M6330415450·"S-II" Chair JEDMED Motor Base 120V

JEDMED

FDA UDI
JEDMED INSTRUMENT COMPANY·M633041545P0·S-II Plus Chair Motor Base 115V

JEDMED

FDA UDI
JEDMED INSTRUMENT COMPANY·M633041545PM0·S-II PLUS CHAIR MOTOR BASE/MOBILE

PIPET CURET

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

VERDICT -II TCA, VERDICT-II MTD

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

21 G X 1.25 IN. BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FMI·May 23, 2017

PINNACLE MTL INS NEUT36IDX58OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·April 8, 2013

ETRAK 2500

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code LLZ·March 24, 2011

VITALITY AVT

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

PLATINUM 1 SERIES

FDA Adverse Event
Malfunction ·ABBOTT MEDICAL OPTICS·Product code KYB·November 20, 2017

PLATINUM 1 SERIES

FDA Adverse Event
Malfunction ·ABBOTT MEDICAL OPTICS·Product code KYB·November 10, 2017

PLATINUM 1 SERIES

FDA Adverse Event
Malfunction ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code KYB·September 17, 2020

UNFOLDER PLATINUM 1 SERIES

FDA Adverse Event
Malfunction ·AMO PUERTO RICO MFG. INC.·Product code KYB·August 9, 2021

PLATINUM 1 SERIES

FDA Adverse Event
Malfunction ·ABBOTT MEDICAL OPTICS·Product code KYB·March 24, 2016

PLATINUM 1 SERIES

FDA Adverse Event
Malfunction ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code KYB·April 4, 2018

PLATINUM 1 SERIES

FDA Adverse Event
Malfunction ·JOHNSON AND JOHNSON SURGICAL VISION, INC.·Product code KYB·April 24, 2018

PLATINUM 1 SERIES

FDA Adverse Event
Malfunction ·JOHNSON AND JOHNSON SURGICAL VISION, INC.·Product code KYB·April 2, 2018

PLATINUM 1 SERIES

FDA Adverse Event
Malfunction ·AMO PUERTO RICO MFG. INC.·Product code KYB·January 11, 2021