30 results · 22ms · 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.

WELL-PEX

FDA 510(k)
FDA Class 2 ·Dental

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014605463·MAQUET 1130 ORTHOPEDIC 4" SOFTCARE

STAR

FDA UDI
Stryker GmbH·00886385017730·Talar A/P Cut Guide Assembly, Right, XS, XXS

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450182239·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450182222·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450182147·

TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) TEST, CATALOG #98000

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

PRIMARY CARE SOLUTIONS STERILE SALINE-0.9% SODIUM CHLORIDE FOR DEVICE IRRIGATION

FDA 510(k)
FDA Class 2 ·General Hospital

QUICK COMBO PAD

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

TRIAGE PROFILER SOB PANEL 25T

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

SERVICE, CCU, HIGH DEF, 560P, 2NDGEN

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code GCJ·May 9, 2016

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

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

QUADRA ASSURA CRT-D, DF4 CONNECTOR

FDA Adverse Event
Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·April 26, 2013

I-STAT EG7+ CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code GKZ·April 6, 2011

CD 3700 SL

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·July 22, 2008