14 results · 21ms · 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.

MEDLINE SUCTION COAGULATOR

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

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970560·

COLONOSCOPY ASSISTANT

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

SYNTHES USS, CLICK'X, USS VAS, DUAL-OPENING USS AND SMALL STATURE USS

FDA 510(k)
FDA Class 2 ·Orthopedic

DEVICE 0175/122949 IMPLANTED 12-AUG-2009

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code LWS·November 10, 2009

CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE PERICARDIAL BIOPROSTHESIS

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·May 21, 2013

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

CAPSUREFIX NOVUS

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011

NEEDLE, HYPODERMIC, SINGLE LUMEN

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·September 1, 2020

TERUMO SURGUARD3 SAFETY HYPODERMIC NEEDLE

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·August 28, 2018

NEEDLE, HYPODERMIC, SINGLE LUMEN

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·November 8, 2019

TERUMO SURGUARD3 SAFETY HYPODERMIC NEEDLE

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·November 13, 2018

SURGUARD3 SAFETY HYPODERMIC NEEDLE

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·December 6, 2024

TERUMO SURGUARD3 SAFETY HYPODERMIC NEEDLE

FDA Adverse Event
Malfunction ·TERUMO PHILIPPINES CORPORATION·Product code FMI·December 2, 2022