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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Portable ECG Monitor

FDA 510(k)
FDA Class 2 ·Cardiovascular

ENTERAL ADMINISTRATION SET WITH SOLUTION CONTAINER, ENTERAL ADMINISTRATION SET, ENTERAL EXTENSION SET WITH MINITUBE CONN

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

RAPHAEL COLOR

FDA 510(k)
FDA Class 2 ·Anesthesiology

WALLSTENT RP ENDOPROSTHESIS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·April 19, 2023

DRUG ELUTING PERMANENT LEFT VENTRICULAR (LV) PACEMAKER ELECTRODE

FDA Adverse Event
Injury ·MPRI·Product code OJX·June 8, 2013

COLLEAGUE PRE 1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011

AXSYM RUBELLA IGG ANTIBODY

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code LFX·September 10, 2008

SENRI

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·April 2, 2021

SENRI

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·July 9, 2019

SENRI

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·July 11, 2024

MERGE HEMO

FDA Adverse Event
Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

MERGE HEMO

FDA Adverse Event
Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

SENRI

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·February 20, 2020

MERGE HEMO

FDA Adverse Event
Malfunction ·MERGE HEALTHCARE·Product code DQK·September 25, 2024

SENRI

FDA Adverse Event
Injury ·KANEKA·Product code LIT·March 12, 2019

SENRI

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·May 6, 2025

MERGE HEMO

FDA Adverse Event
Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

MERGE HEMO

FDA Adverse Event
Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

MERGE HEMO

FDA Adverse Event
Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024

MERGE HEMO

FDA Adverse Event
Malfunction ·MERGE HEALTHCARE·Product code DQK·September 24, 2024