33 results · 32ms · Sources: EU EUDAMED, US FDA

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RESPIFIT S, MODEL RS-LR1001004

FDA 510(k)
FDA Class 2 ·Anesthesiology

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014605678·MAQUET ALPHAMAXX 5.25" SOFTCARE PLUS

DERMAPIK II SKIN TEST SYSTEM, DERMAPIK II (SINGLE TEST DEVICE), POLYPIK II (MULTIPLE SKIN TEST DEVICE), DERMAPIK TRAY, D

FDA 510(k)
FDA Class 2 ·General Hospital

TEMPTELLER INFARED EAR THERMOMETERS, MODEL CT-31/31DX/32/32DX

FDA 510(k)
FDA Class 2 ·General Hospital

PASS LP

FDA Adverse Event
Injury ·MEDICREA INTERNATIONAL·Product code MNI·December 23, 2011

QUICK COMBO PAD

FDA Adverse Event
Injury ·PHYSIO CONTROL CORP.·Product code MLN·January 17, 1997

PASS LP

FDA Adverse Event
Injury ·MEDICREA INTL.·Product code MNI·September 16, 2011

TRIAGE PROFILER SOB PANEL 25T

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·July 19, 2017

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Injury ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·December 13, 2019

TRIAGE PROFILER SOB PANEL 25T

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code JHX·August 29, 2017

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·March 4, 2021

PASS LP

FDA Adverse Event
Injury ·MEDICREA INTL.·Product code MNI·October 14, 2011

PASS LP

FDA Adverse Event
Injury ·MEDICREA INTERNATIONAL·Product code MNI·November 11, 2011

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code DAP·August 3, 2018

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·January 25, 2017

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 23, 2019

AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - POSTERIOR

FDA Adverse Event
Injury ·C.R. BARD, INC.·Product code FTL·April 24, 2013

TRIAGE CARDIOPROFILER TEST

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code MMI·March 31, 2011

POLYFLUX LR CAPILLARY DIALYZER

FDA Adverse Event
Malfunction ·GAMBRO DIALYSATOREN GMBH·Product code MSF·July 24, 2008

PASS LP

FDA Adverse Event
Injury ·MEDICREA INTERNATIONAL·Product code MNI·April 5, 2012