92 results · 57ms · Sources: EU EUDAMED, US FDA

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Crest Medical Limited

Manufacturer
4 Importers

CREST MEDICAL LIMITED

FDA registration
CREST MEDICAL LIMITED·5 products·🇬🇧 United Kingdom

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·November 22, 2013

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 9, 2013

EON

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 18, 2012

EON RECHARGEABLE IPG, 16-CHANNEL

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·December 7, 2015

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 21, 2013

EON RECHARGEABLE IPG, 16-CHANNEL

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 28, 2015

EON MINI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 3, 2014

EON MINI 16-CHANNEL RECHARGEABLE IPG

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 27, 2012

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 6, 2013

EON MINI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 5, 2012

Erich Voss GmbH

Importer
🇩🇪 Germany·1 Manufacturer

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 6, 2013

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 6, 2013

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 7, 2013

DISPOSABLE GROUNDING PAD W/CABLE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.·Product code GXD·July 12, 2017

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 26, 2013

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·June 15, 2016

ON-Q PAINBUSTER

FDA Adverse Event
Other ·I-FLOW CORP.·Product code MEB·February 13, 2007