487 results
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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JOLIFE AB
FDA registration
JOLIFE AB·1 product·🇸🇪 Sweden
LUCAS CPR Chest Compression System
FDA UDI
Jolife AB·00883873834282·LUCAS 3, 3.1, IN SHIPPING BOX, JA
LUCAS™ CHEST COMPRESSION SYSTEM
FDA UDI
Jolife AB·00883873861875·LUCAS 3, 3.0, IN SHIPPING BOX, EN
Lucas Battery Pack
FDA UDI
Jolife AB·00883873970904·LUCAS 2 BATTERY
LUCAS CHEST COMPRESSION SYSTEM
FDA UDI
Jolife AB·00883873861820·LUCAS BATTERY DARK GRAY
LUCAS
FDA UDI
Jolife AB·00883873834329·LUCAS 3, 3.1, IN SHIPPING BOX, EN
LUCAS™ Chest Compression System
FDA UDI
Jolife AB·00883873904565·LUCAS 2, 2.2, IN SHIPPING BOX,EN
Lucas PCI Back Plate
FDA UDI
Jolife AB·00883873948286·LUCAS PCI BACK PLATE
LUCAS CPR CHEST COMPRESSION SYSTEM
FDA Adverse Event
Death
·JOLIFE AB·Product code DRM·December 17, 2014
LUCAS¿ CPR CHEST COMPRESSION SYSTEM
FDA Adverse Event
Injury
·JOLIFE AB - 3005445717·Product code DRM·June 2, 2022
LUCAS 2 Chest Compression System. The device's Instruction for Use is labeled in part: "LUCAS 2 Chest Compression System***jolife***www.lucas-cpr.com***a product by JOLIFE***MANUFACTURER, MAIN OFFICE JOLIFE AB Scheelevagen 17 SE-223 70 LUND Sweden***www.jolife.com***". Designed to uninterrupted chest compressions at a consistent rate and depth.
FDA Recall
Terminated
·Jolife AB Ideon, Scheelev·Product code DRM·February 8, 2011
LUCAS(T) CPR CHEST COMPRESSION SYSTEM
FDA Adverse Event
Injury
·JOLIFE AB·Product code DRM·September 9, 2015
LUCAS¿ CPR CHEST COMPRESSION SYSTEM
FDA Adverse Event
Death
·JOLIFE AB - 3005445717·Product code DRM·June 8, 2018
LUCAS CPR CHEST COMPRESSION SYSTEM
FDA Adverse Event
Malfunction
·JOLIFE AB·Product code DRM·July 1, 2014
LUCAS¿ CPR CHEST COMPRESSION SYSTEM
FDA Adverse Event
Injury
·PHYSIO-CONTROL, INC. - 3015876·Product code DRM·July 12, 2021
LUCAS 3 CHEST COMPRESSION SYSTEM
FDA Adverse Event
Injury
·JOLIFE AB - 3005445717·Product code DRM·July 2, 2025
UNKNOWN_MEDICAL - REDMOND_PRODUCT
FDA Adverse Event
Injury
·JOLIFE AB - 3005445717·Product code DRM·July 2, 2025
LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog Number: 99576-000043 UDI-DI code: 00883873861875 LUCAS 3.1 Model Number: 99576 Catalog Number: 99576-000063 UDI-DI code: 00883873834329 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.
FDA Enforcement
Class II
·Ongoing·Jolife AB·May 20, 2026
LUCAS 2, 3 and 3.1 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.
FDA Enforcement
Class II
·Ongoing·Jolife AB·July 2, 2025
R SERIES DEFIBRILLATOR
FDA Adverse Event
Death
·ZOLL MEDICAL CORPORATION·Product code MKJ·January 20, 2023