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

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GDS-DCS

FDA 510(k)
FDA Class 2 ·Cardiovascular

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450450567·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450407356·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450434369·

EXCEL FRACTURE CEMENTED HIP STEM

FDA 510(k)
FDA Class 2 ·Orthopedic

FAST-CATH 18F HEMOSTASIS INTRODUCER, MODEL 406XXX

FDA 510(k)
FDA Class 2 ·Cardiovascular

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·January 9, 2014

ROD, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

3.0MM TI CERVICAL SPINE LOCKING SCREW 16MM

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code OVE·May 3, 2013

GRANUFLO

FDA Adverse Event
Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·August 28, 2014

3.3MM DRILL 25MM

FDA Adverse Event
Malfunction ·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·May 5, 2011

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·September 25, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·September 26, 2018

UPJ OCCLUSION BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZN·April 7, 2017

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·July 8, 2019

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·November 14, 2017

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·November 19, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·July 19, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·August 1, 2018

UNIVERSA SILICONE FOLEY CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code EZL·August 22, 2018