81 results · 28ms · Sources: EU EUDAMED, US FDA

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MAGSTIM DOUBLE 70-2 COIL

FDA 510(k)
FDA Class 2 ·Neurology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526768475·GENUMEDI PSS GREEN III

ArgenZ HT+ 98x25 ML D4B

FDA UDI
ARGEN CORPORATION, THE·D818130403·Dental porcelain/ceramic restoration kit

EVONOS

FDA UDI
Gyrus ACMI, LLC·00821925016569·GOLDMAN CVD PICK DULL.1 1.2 RAD

VERSANT VALUE

FDA UDI
FGX INTERNATIONAL INC.·00193033307748·

CEFAR REHAB 2 AND REHAB 2 PRO

FDA 510(k)
FDA Class 2 ·Physical Medicine

MASIMO RAINBOW SET PRONTO -7 PULSE CO- OXIMETER AND ACCESSORIES, MODEL PRONTO-7

FDA 510(k)
FDA Class 2 ·Cardiovascular

VALUEBLUE PENCIL, PB VB STERILE

FDA Adverse Event
Malfunction ·ZHEJIANG SHUYOU SURGICAL·Product code GEI·August 30, 2021

VALUEBLUE PENCIL, PB VB STERILE

FDA Adverse Event
Malfunction ·ZHEJIANG SHUYOU SURGICAL·Product code GEI·April 30, 2024

32MM M2A MOD HEAD -6MM NK

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWY·May 24, 2013

E SERIES DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION,·Product code MKJ·August 18, 2008

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011

ALARIS SYSTEM

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·April 13, 2022

INSPIRE 6F

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA - S.R.L.·Product code DTZ·October 28, 2025

RESERVOIR INSPIRE 8

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·May 8, 2026

CAPIOX RX OXYGENATOR

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·May 26, 2023

ADULT DUAL HEATED EVAQUA BREATHING CIRCUIT

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·September 21, 2013

VENTED HUMIDIFICATION CHAMBER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·October 8, 2013

INSPIRE HVR HARDSHELL VENOUS/CARDIOTOMY RESERVOIR

FDA Adverse Event
Injury ·SORIN GROUP ITALIA·Product code DTZ·December 18, 2025

INSPIRE HARD VENOUS RESERVOIR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·July 25, 2022