4,457 results · 23ms · Sources: EU EUDAMED, US FDA

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Unimed

FDA UDI
Unimed Medical Supplies, Inc.·06936735489053·SpO2-Ohrsensor zu Nonin,Sub-D 9pin, 110 cm lang

Unimed

FDA UDI
Unimed Medical Supplies, Inc.·06936735489190·SpO2-Ohrsensor zu Philips / HP Stecker DPK1 12p...

Unimed

FDA UDI
Unimed Medical Supplies, Inc.·06936735488636·SpO2-Ohrsensor zu GE, TruSignal Stecker Sub-D9p...

Unimed

FDA UDI
Unimed Medical Supplies, Inc.·06936735489336·SpO2-Ohrsensor zu Nellcor, St. Sub-D 9pin 110 c...

Unimed

FDA UDI
Unimed Medical Supplies, Inc.·06936735450633·SpO2-Ohrsensor zu CSI / Criticare, Sub-D 9pin r...

buddy,230V SYSTEM

FDA UDI
BELMONT INSTRUMENT CORPORATION·00896128002664·buddy, 230V SYSTEM, GERMAN STANDARD EUROPEAN CORD

SUPPLEMENTARY KIT OUTLINK2

FDA UDI
SWEDEN & MARTINA SPA·D7701168983·SUPPLEMENTARY KIT OUTLINK2 FOR GUIDED SURGERY

840 VENTILATOR

FDA Adverse Event
Malfunction ·PURITAN BENNETT·Product code CBK·July 10, 2007

VITAL SIGNS BREATHING CIRCUITS, EXPANDABLE, ADULT, DISPOSABLE, 1.8 M/72 IN

FDA Adverse Event
Malfunction ·VYAIRE MEDICAL OY·Product code CAI·February 16, 2024

CIRCUIT COAX (A) 2.4M, B.EXT, 2L BAG GSE

FDA Adverse Event
Malfunction ·VYAIRE MEDICAL OY·Product code CAI·August 20, 2022

CERENOVUS NIMBUS GCE

FDA Adverse Event
Malfunction ·NEURAVI LTD.·Product code NRY·June 13, 2022

CO-AXIAL BREATHING CIRCUIT, ADULT, DISPOSABLE, 2.4 M/96 IN

FDA Adverse Event
Injury ·VYAIRE MEDICAL OY·Product code CAI·October 12, 2022

AVEA VENTILATOR

FDA Adverse Event
Malfunction ·CAREFUSION·Product code CBK·March 3, 2016

72`Adult Uni-Lim™, GSE 2 BV Filter 3L

FDA UDI
WESTMED, INC.·00709078002472·72`Adult Uni-Lim™, GSE 2 BV Filter 3L, LF Bag 9...

AVEA VENTILATOR

FDA Adverse Event
Malfunction ·CAREFUSION, INC·Product code CBK·June 1, 2016

GALILEO ECHO

FDA Adverse Event
Malfunction ·IMMUCOR, INC.·Product code KSZ·May 8, 2014

REF 0930 Adult Elongated CO2/O2 Mask, 7' Tubing w/ Threaded Nut, Sivel GSE, 10' GSL X .038" ID X .107" OD, Reflective Luer Connectors, Rx Only, CE0482, (01)00709078005718 - Product Usage: intended to connect with an oxygen source to deliver oxygen therapy to the patient.

FDA Enforcement
Class II ·Terminated·Westmed, Inc.·January 6, 2021

TRANSPOSAL SAFETY STATION NON-STERILE

FDA Adverse Event
Malfunction ·DORNOCH·Product code JCX·August 16, 2017

HUGO¿ RAS SYSTEM

FDA Adverse Event
Malfunction ·SURGICAL·Product code SCV·May 27, 2026

ACUSON REDWOOD ULTRASOUND SYSTEM

FDA Adverse Event
Malfunction ·SIEMENS HEALTHINEERS·Product code IYN·May 9, 2024