19 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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LACEY REVISION FEMORAL COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
Lode B.V.
FDA UDI
Lode B.V.·08717524640194·925900 Excalibur Sport
Lode B.V.
FDA UDI
Lode B.V.·08717524641054·965910 Excalibur Sport
INFRARED LAMP
FDA 510(k)
FDA Class 2
·Physical Medicine
POLAMEDCO TRACHEAL AND NASOTRACHEAL TUBES
FDA 510(k)
FDA Class 2
·Anesthesiology
NA
FDA UDI
STERILMED, INC.·10888551007580·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007573·SAW BLADE SAGITTAL FLARED K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007559·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007566·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007603·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007597·SAW BLADE SAGITTAL K9 K2000 SERIES
COULTER® LH 500 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·January 22, 2013
PLUM A+ DRIVER NEW 8
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FRN·November 8, 2010
QUARTET
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code OJX·July 10, 2014
ABC HANDPIECE LAPAROSCOPIC
FDA Adverse Event
Malfunction
·CONSOLIDATED MEDICAL EQUIPMENT·Product code HAM·February 19, 2019
G7 NEUTRAL E1 LINER 32MM G
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·February 7, 2021
ECHO POR FMRL LAT NC 13X145MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·February 7, 2021
G7 PPS LTD ACET SHELL 58G
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·February 7, 2021
BD Epilor Syringe BD Franklin Lakes, NJ 07417 BD EDC Laagstraat 57, B-9140 Temse-Belgium The Epilor syringe is used in conjunction with an epidural needle with the purpose of finding the epidural space.
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Company·October 2, 2013