23 results · 27ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

NIM Vital, Nerve Integrity Monitor

FDA 510(k)
FDA Class 2 ·Neurology

PATIENT INTERFACE NIM4CPB1 NIM 4.0

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·October 28, 2025

STIMULATOR, ELECTRICAL, EVOKED RESPONSE

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·July 31, 2023

NIM 4.0 CONSOLE

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·September 5, 2025

NIM 4.0 CONSOLE

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·August 2, 2024

NIM 4.0 CONSOLE

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·May 20, 2025

OSTEOTOME, DUNN-DAUTREY 6MM TIP STRAIGHT, T-HANDLE 6-1/2"

FDA UDI
W.H. Holden, Inc.·D9282007590·

PANEL PHOENIX NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·November 9, 2022

7600 SERIES REUSABLE FULL-FACE CPAP/NIPPV MASKS MODELS 7620 LARGE, 7630 MEDIUM, 7640 SMALL, 7650 EXTRA SMALL, 7660 PETIT

FDA 510(k)
FDA Class 2 ·Anesthesiology

Non-contact Infrared Body Thermometer, model:HTD8823US

FDA 510(k)
FDA Class 2 ·General Hospital

PANEL PHOENIX NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·January 10, 2023

PANEL PHOENIX NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·January 10, 2023

PANEL PHOENIX NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·January 10, 2023

PANEL PHOENIX NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·January 10, 2023

PANEL PHOENIX NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·January 10, 2023

PANEL PHOENIX NMIC/ID-307

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·January 10, 2023

COCR HEAD 28/+4 'L' 12/14

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code MEH·January 26, 2026

840 VENTILATOR

FDA Adverse Event
Injury ·COVIDIEN·Product code CBK·October 24, 2014

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·July 27, 2011

RENAISSANCE 26 P-WASS 10/04

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·July 1, 2013