39 results
·
20ms
·
Sources: EU EUDAMED, US FDA
VOLU-SOL HISTO./CYTO. STAIN MOD. #EA65
FDA 510(k)
FDA Class 1
·Hematology
Elite Orthopaedics
FDA UDI
Elite Orthopaedics, Inc.·00816591013387·Post Op Telescoping Knee Brace
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306810077·Blunt Injector, 18G x 7cm, Luer
Elite Orthopaedics
FDA UDI
Elite Orthopaedics, Inc.·00816591013998·OA Knee Brace, Single Upright, Right
Elite Orthopaedics
FDA UDI
Elite Orthopaedics, Inc.·00816591014001·OA Knee Brace, Single Upright, Left
Falcon
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730088604·Bird Beak Pliers w/Cutter
PERI-LOC LOCKING HOLE INSERTS AND CABLE ACCESSORIES
FDA 510(k)
FDA Class 2
·Orthopedic
IGROK
FDA 510(k)
FDA Class 2
·Radiology
PROLENE POLYPROPYLENE SUTURE
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code GAW·May 8, 1998
PLATE CDC ANAEROBE 5% SB 100 EA JP
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·September 9, 2021
PLATE CDC ANAEROBE 5% SB 20 EA
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JSG·June 28, 2021
BIODESIGN URETHRAL SLING
FDA Adverse Event
Injury
·COOK BIOTECH, INC.·Product code PAG·April 3, 2014
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·October 9, 2012
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 28, 2007
SMR HUMERAL HEAD Ø48 MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code KWT·May 8, 2024
SMR REVERSE FINNED HUMERAL BODY
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code PHX·September 29, 2023
PLATE CDC ANAEROBE AGAR 5% SB 90MM 20
FDA Adverse Event
Malfunction
·BECTON DICKINSON GMBH·Product code JSG·February 17, 2022
SMR CEMENTLESS FINNED STEM
FDA Adverse Event
Injury
·LIMACORPORATE SPA·Product code HSD·September 13, 2019
Optiflux F180NR Dialyzers, Catalog Number: 0500318E. Manufactured by Fresenius Medical Care North America, Ogden, UT 84404. Designed for single use acute and chronic hemodialysis.
FDA Recall
Terminated
·Fresenius Medical Care North America·Product code KDI·May 14, 2010
Trinity Biotech, Captia VZV IgG. Product code 2325600: 96 Tests; product code: 2325601: 480 tests. For in vitro diagnostic use. Intended for the detection and quantitative determination of IgG antibody to VZV in human sera.
FDA Recall
Terminated
·Clark Laboratories, Inc. (dba, Trinity Biotech USA)·Product code GQX·May 29, 2012