22 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTHES METALLIC SPIKED WASHERS
FDA 510(k)
FDA Class 2
·Orthopedic
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033521502·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033521571·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033521557·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033521540·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033521564·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033521533·
URETEROSCOPES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PIPELINE FLEX
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·December 16, 2020
PIPELINE FLEX
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·September 21, 2020
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·March 20, 2013
HUDSON ISO-GARD HEPA SMALL STRAIGHT FILTER
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code CAH·February 3, 2011
ACRYSOF TORIC
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·March 14, 2008
AXIOM ARISTOS VX PLUS
FDA Adverse Event
Injury
·SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD·Product code MQB·April 7, 2021
XVIVO Organ Chamber REF 19020
FDA Enforcement
Class II
·Terminated·XVIVO PERFUSION AB·June 8, 2022
SAF-T-INTIMA IV CATHETER SAFETY SYSTEM WITH PRN ADAPTER
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·April 2, 2019
BD SAF-T-INTIMA¿ IV CATHETER SAFETY SYSTEM
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·May 2, 2019
PIPELINE FLEX W/SHIELD TECHNOLOGY
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·February 17, 2021
Breast Biopsy Aiming Device. Magnetic Resonance Imaging System. Model number 5728735
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code LNH·October 5, 2005