23 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Voluntis
FDA registration
Voluntis·2 products·🇫🇷 France
Insulia
FDA UDI
VOLUNTIS·03760261310023·
Insulia
FDA UDI
VOLUNTIS·03760261310061·
HeroTracker Sense
FDA UDI
VOLUNTIS·03760261310184·
Insulia
FDA UDI
VOLUNTIS·03760261310016·
Insulia
FDA UDI
VOLUNTIS·03760261310085·
Insulia
FDA UDI
VOLUNTIS·03760261310009·
Insulia
FDA UDI
VOLUNTIS·03760261310078·
Insulia Diabetes Management Companion
FDA Enforcement
Class II
·Terminated·Voluntis·November 28, 2018
Insulia Diabetes Management Companion
FDA Recall
Terminated
·Voluntis 22 Quai Gallieni Suresnes France·Product code NDC·October 8, 2018
VOLUNTEER PERF KNOXVILLE TN1
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code DWE·March 23, 2015
ADULT CIRCUIT-90" EXP
FDA Adverse Event
Malfunction
·MEDLINE INDUSTRIES, INC.·Product code CAI·February 13, 2007
DREAMSTATION AUTO CPAP
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code BZD·June 24, 2022
HEARTWARE® VENTRICULAR ASSIST SYSTEM
FDA Adverse Event
Malfunction
·HEARTWARE, INC·Product code DSQ·October 3, 2014
TECNIS ITEC PRELOADED 1-PIECE IOL
FDA Adverse Event
Malfunction
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQL·April 28, 2020
ASR ACETABULAR IMPLANT 62
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code JDI·May 11, 2018
HAMILTON G5
FDA Adverse Event
Injury
·HAMILTON MEDICAL AG·Product code CBK·February 11, 2025
ASR UNI FEMORAL IMPL SIZE 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·November 1, 2016
ASR UNI FEMORAL IMPL SIZE 41
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·April 25, 2012
V40 COCR LFIT HEAD 36MM/+5
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·September 28, 2018