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

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MODOFOCATION TO SYNTHES ANKLE ARTHRODESIS PLATES

FDA 510(k)
FDA Class 2 ·Orthopedic

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·H65810222551·Ultra Clean Powder

Reicodent

FDA UDI
devemed GmbH·04061644047901·Tweezers "College" | 15.0 cm angled Handle serr...

MEDTRONIC SOFAMOR DANEK CEMENT RESTRICTOR

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

LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE (MADGIC)

FDA 510(k)
FDA Class 2 ·Anesthesiology

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·March 26, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 28, 2011

MICROSTAAR INJECTOR

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code MSS·March 26, 2008

RANGER PACLITAXEL-COATED PTA BALLOON CATHETER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code ONU·September 29, 2022

RANGER PACLITAXEL-COATED PTA BALLOON CATHETER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code ONU·September 29, 2022

RANGER PACLITAXEL-COATED PTA BALLOON CATHETER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code ONU·September 29, 2022

ELITE 12CM STRAIGHT ATTACHMENT

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code HBE·January 22, 2021

Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012

The Propaq LT Series monitors. Model numbers 802LTAN, 802LT0N, and 802LTRN. These devices are indicated for ECG, noninvasive blood pressure (NIBP), respiration and SpO2. The most likely locations for patients to be monitored by these devices are hospital general medical-surgical, telemetry, and intermediate care floors, hospital emergency departments, transport, emergency medical services, and other healthcare applications. intended to be used by clinicians and medically qualified personnel for single or multiparameter vital signs monitoring of ambulatory and nonambulatory patients, including neonate, pediatric and adult patients. These devices are indicated for ECG, noninvasive blood pressure (NIBP), respiration and SpO2. The most likely locations for patients to be monitored by these devices are hospital general medicalsurgical, telemetry, and intermediate care floors, hospital emergency departments, transport, emergency medical services, and other healthcare applications. The monitors can be used as stand-alone devices or as devices networked to an Acuity Central Station through wireless communication over a Welch Allyn FlexNet network.

FDA Enforcement
Class II ·Terminated·Welch Allyn Protocol, Inc·January 15, 2014