18 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Always/Tampax bladder supports
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ECHO FX HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304520318·
ProLift Trial
FDA UDI
Life Spine, Inc.·00190837087555·
EUROMI EVA SP6
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
3-Lead,ECG,Univ,Pinch,18",IEC
FDA UDI
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904059341·
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code DZL·December 23, 2014
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code JEY·December 23, 2014
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code DZL·December 23, 2014
ILAB? POLARIS MULTI-MODALITY GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQK·May 14, 2026
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 30, 2013
VITALITY
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 6, 2011
ONE TOUCH ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·September 4, 2008
GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 7 L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·June 28, 2022
D902 LILLIPUT ECMO M PHISIO
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·April 7, 2022
LILLIPUP PMP, LILLIPUT PMP INTEGRATED
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·June 27, 2022
36MM COCR MOD HD STD
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JDI·January 19, 2021
Medical Linear Accelerator
FDA Enforcement
Class II
·Terminated·Elekta, Inc.·September 14, 2016