31 results · 25ms · Sources: EU EUDAMED, US FDA

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FIBREX CATHETER PATENCY DEVICE

FDA 510(k)
FDA Class 2 ·General Hospital

NA

FDA UDI
GE Healthcare Finland Oy·00840682104456·

NA

FDA UDI
GE Healthcare Finland Oy·00840682104432·

NA

FDA UDI
GE Healthcare Finland Oy·00840682104463·

NA

FDA UDI
GE Healthcare Finland Oy·00840682104425·

Myo/Wire II

FDA UDI
A & E MEDICAL CORPORATION·10841291104834·SS Suture, 4 per sleeve

LORENZ FIDUCAIL SCREW

FDA 510(k)
FDA Class 2 ·Neurology

AB BELT

FDA 510(k)
FDA Class 2 ·Physical Medicine

ASR ACETABULAR CUPS 58

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·April 11, 2012

ASR ACETABULAR CUPS 48

FDA Adverse Event
Injury ·DEPUY INTL, LTD.·Product code KWA·December 29, 2010

ONIPOD INSULIN PUMP

FDA Adverse Event
Malfunction ·INSULET CORP·Product code LZG·March 12, 2013

840 VENTILATOR

FDA Adverse Event
Malfunction ·PURITAN-BENNETT IRELAND·Product code CBK·May 7, 2008

PRECISION XTRA

FDA Adverse Event
Malfunction ·Product code NBW·April 5, 2011

ASR UNI FEMORAL IMPL SIZE 51

FDA Adverse Event
Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·August 21, 2013

ASR ACETABULAR CUPS 60

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·October 24, 2015

ASR ACETABULAR CUPS 58

FDA Adverse Event
Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·August 21, 2013

ASR UNI FEMORAL IMPL SIZE 49

FDA Adverse Event
Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 22, 2013

ADAPTER SLEEVES 12/14 +8

FDA Adverse Event
Injury ·DEPUY INTL.,LTD 8010379·Product code KWA·November 4, 2015

ADAPTER SLEEVES

FDA Adverse Event
Injury ·DEPUY INTL.,LTD 8010379·Product code KWA·February 2, 2016

ASR ACETABULAR CUPS 56

FDA Adverse Event
Injury ·DEPUY INTL.,LTD 8010379·Product code KWA·February 2, 2016