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

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EKG-PLUS II SOFTWARE

FDA 510(k)

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450209233·

STAT PROFILE PHOX PLUS ANALYZER

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

ALLOMATRIX MODEL# 86

FDA 510(k)
FDA Class 2 ·Orthopedic

TRUEBALANCE

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·April 29, 2015

TRUEBALANCE

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·August 13, 2014

LUX 1440

FDA Adverse Event
Malfunction ·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012

TRUE BALANCE

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·February 21, 2014

TRUEBALANCE

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·September 16, 2014

TRUEBALANCE

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·October 31, 2014

TRUEBALANCE

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·October 31, 2014

TRUEBALANCE

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·January 22, 2015

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 2, 2013

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·September 15, 2014

CITATION TMZF HA STEM #6 LEFT

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS CORK·Product code JDI·May 12, 2011

DIDECO COMPACTFLO EVOLUTION OXYGENATOR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA·Product code DTZ·January 15, 2016

Custom Cardiac Cath Pack Kit, K09-08945, Sterile EO, Merit Medical Systems, Inc., South Jordan, Utah 84095. Intended for fluid management convenience when catheterization is required.

FDA Recall
Terminated ·Merit Medical Systems, Inc.·Product code OEZ·January 29, 2009