17 results · 24ms · Sources: EU EUDAMED, US FDA

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VELASHAPE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ULTRA-HIGH ENERGY GENERAL PURPOSE COLLIMATOR (UHGP) [FOR CARDIAC IMAGING]

FDA 510(k)
FDA Class 2 ·Radiology

I.V. SET-LUER LOCK WITH LATEX FREE INJECTION SITE, MODEL B411

FDA 510(k)
FDA Class 2 ·General Hospital

INFINION CX

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 14, 2021

WAVEWRITER ALPHA PRIME

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 19, 2023

10MM/130 DEG TI CANN TROCH FIXATION NAIL 170MM

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code HSB·April 22, 2013

ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLE

FDA Adverse Event
Injury ·COVIDIEN SURGICAL SUPPLY·Product code GAA·April 21, 2011

GEN2 ADJUSTABLE GASTRIC BAND - 11 CM, UNLOCKA

FDA Adverse Event
Malfunction ·OBTECH MEDICAL SARL·Product code LTI·July 9, 2008

CAPIOX FX OXYGENATOR

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·May 22, 2025

CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 5, 2022

CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 16, 2022

CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·May 24, 2022

CAPIOX FX05 OXYGENATOR

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·May 19, 2023

CAPIOX FX25 OXYGENATOR

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 11, 2022

CAPIOX FX25 OXYGENATOR

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 11, 2022

CAPIOX FX25 OXYGENATOR

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 29, 2022

CAPIOX FX25 OXYGENATOR

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·February 14, 2022