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

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Powder Free Nitrile Examination Gloves, Orange

FDA 510(k)
FDA Class 1 ·General Hospital

Certi-Strips - Woven - Fingertip - 25/Box

FDA UDI
Certified Safety Manufacturing, Inc.·00766588202297·Certi-Strips - Woven - Fingertip - 25/Box

R & D BODY FLUID CONTROL

FDA 510(k)
FDA Class 2 ·Hematology

ENVOY DISTAL ACCESS GUIDING CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

BD® BLUNT FILL NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·June 20, 2022

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 29, 2023

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 24, 2023

QUATRODE

FDA Adverse Event
Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code GZB·September 18, 2013

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 20, 2023

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 23, 2023

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 6, 2022

CONTOUR TEST STRIPS (50)

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·December 12, 2008

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·May 27, 2022

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 30, 2024

QUATTRODE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·September 18, 2013

QUATTRODE

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·September 18, 2013

PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES

FDA Adverse Event
RESPIRONICS INC·Product code BTI·November 3, 2014

MINICAP TRANSFER SET

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·August 23, 2011

DURATA STS OPTIM PASSIVE FIXATION, DF4 CONNECTOR

FDA Adverse Event
Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·July 11, 2013

CONTEGRA PULMONARY VALVED CONDUIT

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code MWH·May 24, 2021