55 results · 20ms · Sources: EU EUDAMED, US FDA

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Spectra Optia Apheresis System

FDA 510(k)
FDA Unclassified ·Unknown

Epredia

FDA UDI
SHANDON DIAGNOSTICS LIMITED·05051663517751·CTM6 coverslipper- Accessory

BR2000 BLADES

FDA UDI
Peter Brasseler Holdings, LLC·00887919100812·K7-2590-47

Brasseler

FDA UDI
Provision·B504OMK72590500·

Brasseler

FDA UDI
Provision·B504OMK72590470·

NA

FDA UDI
STERILMED, INC.·10888551007511·SAW BLADE OSCILLATING AGGRESSIVE CUT LARGE BONE

NA

FDA UDI
STERILMED, INC.·10888551007504·SAW BLADE OSCILLATING AGGRESSIVE CUT LARGE BONE

INSPIRATION; VENTILATOR SYSTEM, LS VENTILATOR SYSTEM, INFANT VENTILATOR SYSTEM AND INFANT LS VENTILATOR SYSTEM

FDA 510(k)
FDA Class 2 ·Anesthesiology

FLEBOSET DOUBLE

FDA 510(k)
FDA Class 2 ·General Hospital

ITREL 3

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·June 17, 2013

PULSE GEN MODEL 102R

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·July 20, 2011

PROGRAMMING WAND

FDA Adverse Event
Malfunction ·CYBERONICS, INC.·Product code LYJ·September 19, 2008

RADIFOCUS GLIDEWIRE ADVANTAGE

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 1, 2020

GLIDEWIRE ADVANTAGE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 9, 2025

RADIFOCUS GLIDEWIRE ADVANTAGE

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 23, 2022

CAPIOX RX OXYGENATOR

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·March 28, 2019

RADIFOCUS GLIDEWIRE ADVANTAGE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 3, 2025

RADIFOCUS GUIDEWIRE ADVANTAGE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 12, 2024

RADIFOCUS GLIDEWIRE ADVANTAGE

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DQX·August 30, 2023

RADIFOCUS GLIDEWIRE ADVANTAGE

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·August 7, 2020