66 results · 23ms · 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.

LIFECHOICE OXYGEN CONCENTRATOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

RESUSCITATION UNIT 105

FDA 510(k)
FDA Class 2 ·Anesthesiology

TEKMEDIC POWDER-FREE WITH PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS)

FDA 510(k)
FDA Class 1 ·General Hospital

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·July 22, 2015

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·June 18, 2015

PENUMBRA SYSTEM JETD REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·May 8, 2019

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·July 17, 2015

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·October 30, 2015

PENUMBRA SYSTEM 3MAX REPERFUSION CATHETER

FDA Adverse Event
Injury ·PENUMBRA, INC.·Product code NRY·June 14, 2015

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·June 26, 2015

EZ BREATHE ATOMIZER

FDA Adverse Event
HEALTH & LIFE (SUZHOU) CO., LTD.·Product code CCQ·April 12, 2013

PINNACLE MTL INS NEUT36IDX56OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·May 20, 2011

VERSYS HIP SYSTEM FEMORAL STEM BEADED FULLCOAT COLLARED

FDA Adverse Event
Malfunction ·ZIMMER, INC.·Product code KWY·August 12, 2008

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·June 9, 2015

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·September 9, 2015

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·September 16, 2015

PENUMBRA SYSTEM 4MAX REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·July 30, 2015

PENUMBRA SYSTEM JETD REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·November 11, 2021

PENUMBRA SYSTEM 4MAX REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·October 16, 2015

PENUMBRA SYSTEM 5MAX ACE REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·June 18, 2015