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

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Zio AT ECG Monitoring System, ZEUS System

FDA 510(k)
FDA Class 2 ·Cardiovascular

AqWire

FDA UDI
Covidien LP·10821684007164·Hydrophilic Guidewire

AqWire

FDA UDI
Covidien LP·00821684058541·Hydrophilic Guidewire

ZenFlex

FDA UDI
Kerr Corporation·00195062029752·Rotary Files

Life Instruments

FDA UDI
Life Instrument Corporation·M930718150200·Down Pushing Curette #2

PYRENEES Cervical Plate System

FDA UDI
VB Spine LLC·10888857273832·Stop Drill, Size Dia. 2.5x12 mm

OrthoMedFlex

FDA UDI
ORTHOMEDFLEX LLC·M7161111815020·Standard Offset, Collared Stem, Size 15

BD VACUTAINER RAPID SERUM TUBE BLOOD COLLECTION TUBE, MODEL 368774

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

STREAMLINE TL SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 9, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 1, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 22, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·June 8, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·April 26, 2018

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·April 20, 2018

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·March 24, 2022

BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 22, 2018

530G INSULIN PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 17, 2014

CORE SUMEX

FDA Adverse Event
STRYKER INSTRUMENTS·Product code HBE·June 11, 2013

INSTATRAK 3500

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code LLZ·July 7, 2011