38 results · 22ms · 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.

MICROSCAN SYNERGIES PLUS GRAM POSITIVE MIC/COMBO PANELS NEW ANTIMICROBIAL-GENTAMICIN SYNERGY SCREEN

FDA 510(k)
FDA Class 2 ·Microbiology

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690191711·Modular Tibia Impactor Pad (Blue)

MULTIRATE INFUSOR SV; MULTIRATE INFUSER LV; BAXTER PAIN MATE PAIN MANAGEMENT SYSTEM

FDA 510(k)
FDA Class 2 ·General Hospital

ARIA

FDA 510(k)
FDA Class 2 ·Cardiovascular

SPECTRA WAVEWRITER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 16, 2024

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 26, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

S5 ROLLER PUMP

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SYSTEM

FDA Adverse Event
Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

S5 SENSOR MODULE FOR BUBBLE DETECTOR

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTW·October 21, 2016

INFUSOR

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code MEB·September 17, 2021

CARE ASSIST BED

FDA Adverse Event
Malfunction ·HILL-ROM PLUVIGNER·Product code FNL·April 9, 2013

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·April 28, 2011

XACT CAROTID STENT SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR GALWAY·Product code NIM·July 8, 2008

LCD TOUCHSCREEN, RP150, S5

FDA Adverse Event
Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 14, 2012