27 results · 23ms · Sources: EU EUDAMED, US FDA

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LeadCare Plus Blood Lead Testing System

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613084844·Tabb Flap Knife, Double Ended, 0.9 x 1mm Blade,...

DISPOSABLE NON-ADHESIVE SPO2 SENSORS

FDA 510(k)
FDA Class 2 ·Cardiovascular

ARMADA 14 PTA CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·December 15, 2020

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·August 24, 2020

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 6, 2020

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 7, 2020

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 14, 2023

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 9, 2020

6800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 24, 2013

HEARTSTART ONSITE

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 26, 2014

CAPSURE SP

FDA Adverse Event
Injury ·MPRI·Product code DTB·October 10, 2015

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·March 8, 2021

NI

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·June 8, 2021

NI

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·February 18, 2022

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 20, 2023

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 24, 2023

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 19, 2021

MINICAP

FDA Adverse Event
Malfunction ·VANTIVE US HEALTHCARE LLC·Product code KDJ·March 30, 2026