16 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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TISSUE-TEK IMMUNOHISTOLOGY KIT LYSOZZM
FDA 510(k)
FDA Class 2
·Immunology
E-Shield Multi-paried Subdermal Needle Electrodes
FDA 510(k)
FDA Class 2
·Neurology
DUREX SPEARMINT SCENTED LUBRICATED LATEX CONDOM (DUREX 'TINGLING PLEASURE' CONDOM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
36CM PERM CATH KIT X5
FDA Adverse Event
Malfunction
·COVIDIEN·Product code MSD·February 20, 2014
ZEPHYR XL DR
FDA Adverse Event
Death
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWP·November 21, 2012
4.0MM CANC LOCK SCRW 44MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code HRS·September 17, 2010
UNK HIP FEMORAL HEAD METAL ASR
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023
UNK HIP FEMORAL SLEEVE ASR
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023
UNKNOWN HIP FEMORAL STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 7, 2023
UNK HIP FEMORAL SLEEVE ASR
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023
UNK HIP FEMORAL HEAD METAL ASR
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023
UNK HIP ACETABULAR CUP ASR
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023
UNKNOWN HIP FEMORAL STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 7, 2023
UNKNOWN HIP FEMORAL STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 7, 2023
UNK HIP ACETABULAR CUP ASR
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·July 7, 2023
Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The Flexor¿ Radial Hydrophilic Introducer Access Set is intended to introduce diagnostic and interventional devices In radial artery access procedures
FDA Enforcement
Class II
·Terminated·Cook Inc.·March 8, 2017