22 results · 21ms · Sources: EU EUDAMED, US FDA

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CIRCUFLOW 5150

FDA 510(k)
FDA Class 2 ·Cardiovascular

AMS INTEPRO Y-MESH

FDA Adverse Event
Death ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTP·June 11, 2014

JEROME GLASS RING

FDA 510(k)
FDA Class 2 ·Neurology

BIOPLEX 2200 HSV-1 AND HSV-2 IGG KIT

FDA 510(k)
FDA Class 2 ·Microbiology

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172973295·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970584·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970690·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970676·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970645·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970621·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970638·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970591·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970683·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970652·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970560·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970669·

SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·May 22, 2013

OT VERIO SYNC METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 27, 2014

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011

UNITIP CATHETER FOR HR GI

FDA Adverse Event
Injury ·UNISENSOR AG·Product code FFX·August 25, 2014