76 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.

Adcura® Sagittae® Lateral Lumbar Interbody Fusion Devices

FDA 510(k)
FDA Class 2 ·Orthopedic

K-Systems

FDA UDI
Coopersurgical, Inc.·00888937025040·G73 Dry Bath Incubator

REAMER HEAD 6.5mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665000573·

CATHETER CONNECTIONS DUALCAP SOLO

FDA 510(k)
FDA Class 2 ·General Hospital

CYCLOSPORINE (CSA) FLEX REAGENT CARTRIDGE

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

HOMECHOICE, DOMESTIC 120V

FDA Adverse Event
BAXTER HEALTHCARE·Product code FKX·June 11, 2008

HOMECHOICE, DOMESTIC 120V

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·July 24, 2009

PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

HOMECHOICE CYCLER-REFURBISHED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·December 4, 2007

HOMECHOICE CYCLER-REFURBISHED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·December 10, 2007

PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 27, 2008

PD CYCLER 110 VOLT HOME CHOCIEPRO AUTOMATED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

HOMECHOICE CYCLER-REFURBISHED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·May 13, 2008

HOMECHOICE CYCLER -REFURBISHED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 5, 2008

HOMECHOICE CYCLER REFURBISHED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·March 6, 2008

RIATA ACTIVE FIXATION

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·November 10, 2008

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 10, 2011

EON MINI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 10, 2013