30 results · 33ms · Sources: EU EUDAMED, US FDA

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CRF Radiofrequency Ablation System

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

IROOT BP PLUS

FDA 510(k)
FDA Class 2 ·Dental

REGIONAL OXIMETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 3, 2024

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

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·October 22, 2014

1 QUART SHARPS CONTAINER

FDA Adverse Event
Malfunction ·SHARPS COMPLIANCE, INC.·Product code FMI·July 26, 2011

EVIA DR-T PROMRI

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·October 30, 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