35 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Voluntis
Manufacturer
🇫🇷 France·1 Basic UDI-DI·2 Devices
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·
Respi.Me
Device
EU MDR
·
Eu Md Class 1
·Voluntis·On the market
Respi.Me
Device
EU MDR
·
Eu Md Class 1
·Voluntis·On the market
Respi.Me
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Voluntis·2 devices
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
BoLCA ESTHIA VOLUPTY FILL MILD
Device
EU MDD
·
Eu Md Class 3
·BioPlus Co., Ltd.·On the market·2 countries
BoLCA ESTHIA VOLUPTY FILL FIRM
Device
EU MDD
·
Eu Md Class 3
·BioPlus Co., Ltd.·On the market·2 countries
BoLCA ESTHIA VOLUPTY FILL MILD
Device
EU MDD
·
Eu Md Class 3
·BioPlus Co., Ltd.·On the market·2 countries
BoLCA ESTHIA VOLUPTY FILL FIRM
Device
EU MDD
·
Eu Md Class 3
·BioPlus Co., Ltd.·On the market·2 countries
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