21 results
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60ms
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Sources: EU EUDAMED, US FDA
Sentinel Medical Technologies, LLC
Manufacturer
🇺🇸 United States
SENTINEL MEDICAL TECHNOLOGIES, LLC
FDA registration
SENTINEL MEDICAL TECHNOLOGIES, LLC·2 products·🇺🇸 United States
TraumaGuard Intra-abdominal Pressure-Sensing System
FDA UDI
SENTINEL MEDICAL TECHNOLOGIES·00860003478776·The Reusable Temperature Cable connects to a te...
TraumaGuard Intra-abdominal Pressure-Sensing System
FDA UDI
SENTINEL MEDICAL TECHNOLOGIES·00860003478745·The Reusable Temperature Cable connects to a te...
TraumaGuard Intra-abdominal Pressure-Sensing System
FDA UDI
SENTINEL MEDICAL TECHNOLOGIES·00860003478714·The Reusable Temperature Cable connects to a te...
TraumaGuard Intra-abdominal Pressure-Sensing System
FDA UDI
SENTINEL MEDICAL TECHNOLOGIES·00860011933106·The Reusable Temperature Cable connects to a te...
TraumaGuard Intra-abdominal Pressure-Sensing System
FDA UDI
SENTINEL MEDICAL TECHNOLOGIES·00860003478738·The Reusable Temperature Cable connects to a te...
TraumaGuard Intra-abdominal Pressure-Sensing System
FDA UDI
SENTINEL MEDICAL TECHNOLOGIES·00860003478707·TraumaGuard Intra-abdominal Pressure-Sensing Ca...
TraumaGuard Intra-abdominal Pressure-Sensing System
FDA UDI
SENTINEL MEDICAL TECHNOLOGIES·00860003478721·The Reusable Temperature Cable connects to a te...
TraumaGuard Intra-abdominal Pressure-Sensing System
FDA UDI
SENTINEL MEDICAL TECHNOLOGIES·00860003478752·The Reusable Temperature Cable connects to a te...
BD PYXIS¿ ES SERVER
FDA Adverse Event
Malfunction
·CAREFUSION 303, INC.·Product code BRY·June 23, 2025
BD PYXIS¿ ES SERVER
FDA Adverse Event
Malfunction
·CAREFUSION 303, INC.·Product code BRY·June 23, 2025
VITEK MS INSTRUMENT ®
FDA Adverse Event
Malfunction
·BIOMERIEUX, SA·Product code QBN·March 1, 2023
KANGAROO
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code KNT·July 25, 2023
INSYTE AUTOG BC BLU 22GA X 1.0IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 28, 2020
Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is easy to install and to use.
FDA Recall
Terminated
·Spacelabs Healthcare, Ltd. Unit B Foxholes Centre; John Tate Road Hertford United Kingdom·Product code DQK·November 6, 2020
BD PYXIS¿ MEDSTATION¿ ES
FDA Adverse Event
Malfunction
·CAREFUSION 303, INC.·Product code BRY·July 30, 2025
ALLURA XPER FD20
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code OWB·October 19, 2018
Obelis s.a.
Authorized representative
🇧🇪 Belgium·546 Manufacturers·18515 Devices
Emergo Europe B.V.
Authorized representative
🇳🇱 Netherlands·900 Manufacturers·22100 Devices