213 results · 23ms · Sources: EU EUDAMED, US FDA

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VORTRAN GO2VENT with PEEP Valve

FDA 510(k)
FDA Class 2 ·Anesthesiology

Nucleus

FDA UDI
COCHLEAR LIMITED·09321502017756·Cochlear Nucleus CP800 Series Compact Rechargea...

IDB 3

FDA UDI
Sprintray, Inc.·00850070544832·SprintRay IDB 3 is a light-curable polymerizabl...

VEO® Lateral Interbody Fusion System

FDA UDI
Choice Spine, LP·00840996132749·LATERAL,NERVE RETRACTOR

WANDY SELF-ADHESIVE NEUROSTIMULATION ELECTRODE

FDA 510(k)
FDA Class 2 ·Neurology

EXOMIO, MODEL 1.1

FDA 510(k)
FDA Class 2 ·Radiology

670G INSULIN PUMP MMT-1780KL

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·December 5, 2022

MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 22, 2023

AUTOMATED IMPELLA CONTROLLER

FDA Adverse Event
Malfunction ·ABIOMED, INC.·Product code OZD·November 3, 2024

630G INSULIN PUMP MMT-1715K 630G BLACK MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·January 25, 2022

PUMP MMT-1712KL 640G V4.10 BK SF MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 14, 2022

670G INSULIN PUMP MMT-1780KL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·April 14, 2022

PUMP MMT-1782K 670G V4.11 MM

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 3, 2022

PUMP MMT-1711KL 640G V4.10 BK SF MM

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 24, 2022

630G INSULIN PUMP MMT-1715K 630G BLACK MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·February 1, 2022

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 1, 2021

MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 12, 2023

PROLIEVE THERMODILITATION KIT

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·October 16, 2008

840 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 28, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 5, 2011