18 results · 26ms · Sources: EU EUDAMED, US FDA

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LRTM SURGICAL MESH

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MESH, SURGICAL

FDA Adverse Event
Injury ·W. L. GORE AND ASSOCIATES, INC.·Product code FTM·August 12, 2023

TruForm

FDA UDI
Rmo, Inc.·00885797100023·MN 1MOL BD KT STD NO/L R&L 176

PORTRAIT FEMORAL COMPONENT

FDA 510(k)
FDA Class 2 ·Orthopedic

SYNTHES (USA) RESORBABLE TACK SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

SYRINGE 0.5ML 31GA 8MM UFII 10BAG 500CS

FDA Adverse Event
Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·September 6, 2019

ETEST FLUCONAZOLE FL 256 WW S30

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

ETEST FLUCONAZOLE FL 256 WW S30

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

ETEST FLUCONAZOLE FL 256 WW S30

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

ETEST FLUCONAZOLE FL 256 WW S30

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

ETEST FLUCONAZOLE FL 256 WW S30

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

ETEST FLUCONAZOLE FL 256 WW S30

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

ETEST FLUCONAZOLE FL 256 WW S30

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

ETEST FLUCONAZOLE FL 256 WW S30

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

1.8MM UNIVERSAL VARIABLE ANGLELOCKING DRILL GUIDE

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code FZX·April 22, 2013

BGR, ANTI-D (MONOCLONAL) (IGG BLEND)

FDA Adverse Event
Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code KSZ·March 30, 2011

MAMMOMARK2 8 MR BIOSITE INDENT

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 2, 2008

Ellipse, Sterile EO, Model #/ Part #: CD1275-36/100116115; CD1275-36Q/100116116; CD1277-36/100048388, 100048391, 100060126, 100116208, 10011636; CD1277-36Q/100048374, 100048394, 100060198, 100098497, 100116268, 100116345; CD1293-36Q/100057838; CD1309-36/100057717; CD1309-36Q/100057718; CD1311-36/100057802, 100060153; CD1311-36Q/100057803, 100060174, 100116264; CD1377-36/100078796, 100079180, 100096847; CD1377-36C/100078612, 100079197, 100079368, 100116120, 100116407, 100116447; CD1377-36Q/100078747, 100079210, 100096848, 100116385, 100116423, 100116427; CD1377-36QC/100078602, 100079199, 100079229, 100116398, 100116409, 100116466,100116485, 100127151, 100127152, 100127153; CD1393-36C/100116461; CD1393-36QC/100080656, 100116339; CD1409-36Q/100080251; CD1411-36C/100080197, 100080232, 100116411, 100116481; CD1411-36Q/100080244, 100080245, 100116338, 100116464; CD1411-36QC/100116337; CD2275-36/100116355; CD2275-36Q/100116349; CD2277-36/100048359, 100048402, 100116206, 100116207; CD2277-36Q/100048377, 100048404,100060190, 100098661, 100116342, 100116350; CD2293-36/100057765; CD2293-36Q/100057766; CD2309-36/100057804; CD2309-36Q/100057763; CD2311-36/100057679, 100060100; CD2311-36Q/100057835, 100060161, 100116351; CD2377-36/100078811, 100079226, 100096774; CD2377-36C/100078601,100079225, 100079304, 100116405, 100116424, 100116484; CD2377-36Q/100078812,100079208, 100096838, 100116406, 100116414, 100116437; CD2377-36QC/100078579, 100079176, 100079352, 100116413, 100116422, 100116436, 100116482, 100127100, 100127154, 100127181; CD2393-36C/100080653, 100116416; CD2393-36QC/100080655, 100116451; CD2409-36C/100079997; CD2409-36Q/100080149; CD2411-36C/100079986, 100080104, 100116118, 100116444; CD2411-36Q/100080180, 100080230, 100116370, 100116420

FDA Enforcement
Class II ·Terminated·St Jude Medical Inc.·July 4, 2018