10,000 results
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100ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FDA UDI
Fehling Instruments GmbH & Co. KG·04058749070132·CERAMO raspatory, curved, 6 x 190 mm
NEURORECOVERY, INC. (NRI) COMPREHENSIVE INTRACRANIAL PRESSURE EVALUATION AND RELIEF (CIPER) KIT
FDA 510(k)
FDA Class 2
·Neurology
NRI FOWLER BACK STRETCHER
FDA Adverse Event
Injury
·BIODEX MEDICAL SYSTEMS, INC.·Product code FPO·November 18, 2015
MITEK CUFFTACK SUTURLESS ANCHOR
FDA Adverse Event
Injury
·MITEK WORLDWIDE·Product code MAI·August 20, 2003
HIRES 90K
FDA Adverse Event
Injury
·ADVANCED BIONICS CORP.·Product code MCM·September 21, 2007
ADVANCED BIONICS HIRES ULTRA 3D CI
FDA Adverse Event
Malfunction
·ADVANCED BIONICS LLC.·Product code MCM·September 24, 2024
PENUMBRA SYSTEM MAX ASPIRATION TUBING
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·June 24, 2015
CLARION
FDA Adverse Event
Injury
·ADVANCED BIONICS CORP.·Product code MCM·September 22, 2004
HIRES¿ 90K
FDA Adverse Event
Injury
·ADVANCED BIONICS, LLC·Product code MCM·December 13, 2024
PENUMBRA SYSTEM ASPIRATION PUMP MAX 220
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·April 9, 2018
132CM LARGE BORE 71 CATHETER
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code NRY·August 1, 2024
UNK CONCORDE CAGE
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SÃ RL CH·Product code MQP·June 30, 2021
THERMOCOOL® SMART TOUCH¿ BI-DIRECTIONAL NAVIGATION CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·October 7, 2024
PENUMBRA SYSTEM ASPIRATION PUMP MAX 110V
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code DXE·November 2, 2016
DEPUY ASR XL FEM IMP SIZE 41
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·June 10, 2021
ASR ACETABULAR IMPLANT 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·June 10, 2021
LARGE MOD HEAD ADAPT 12/14 +5
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·June 10, 2021
CARPENTIER-EDWARDS PERIMOUNT MAGNA MITRAL PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·April 24, 2014
132CM LARGE BORE 71 CATHETER
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code NRY·July 9, 2024
132CM LARGE BORE 71 CATHETER
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code NRY·July 11, 2024