24 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
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