815 results
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35ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Vapotherm
FDA UDI
VAPOTHERM, INC.·00841737101352·Precision Flow Heliox
ARROW
FDA UDI
TELEFLEX INCORPORATED·00801902073846·Pressure Injectable Multi-Lumen Central Venous ...
ARROW
FDA UDI
TELEFLEX INCORPORATED·10801902115710·Pressure Injectable Multi-Lumen Central Venous ...
Vapotherm
FDA UDI
VAPOTHERM, INC.·00841737101222·Precision Flow Heliox Startup Kit, Europe
Vapotherm
FDA UDI
VAPOTHERM, INC.·00841737101239·Precision Flow Heliox Startup Kit, United Kingdom
Vapotherm
FDA UDI
VAPOTHERM, INC.·00841737101246·Precision Flow Heliox Startup Kit, United States
Vapotherm
FDA UDI
VAPOTHERM, INC.·00841737102083·Precision Flow Startup Kit, Israel
Vapotherm
FDA UDI
VAPOTHERM, INC.·00841737103264·Precision Flow Heliox, Brazil Unit
Vapotherm
FDA UDI
VAPOTHERM, INC.·00841737105015·Precision Flow Heliox 4th Ed, South Africa
Vapotherm
FDA UDI
VAPOTHERM, INC.·00841737102090·Precision Flow Heliox Startup Kit, Turkey
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·August 1, 2012
QUANTUM PERFUSION CENTRIFUGAL BLOOD PUMP CP22 WITH INTEGRATED SENSORS
FDA Adverse Event
Death
·SPECTRUM MEDICAL S.R.L.·Product code KFM·December 24, 2025
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORP.·Product code DSQ·September 9, 2013
HEARTMATE 3 LVAS IMPLANT KIT
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·February 21, 2022
HEARTMATE II LVAS IMPLANT KIT
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·May 4, 2021
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORP.·Product code DSQ·January 29, 2014
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·June 28, 2017
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·September 6, 2012
Vapotherm
FDA UDI
VAPOTHERM, INC.·00841737102755·Precision Flow Heliox UKIT, Germany
Vapotherm
FDA UDI
VAPOTHERM, INC.·00841737102731·Precision Flow Heliox UKIT, US