9 results · 21ms · Sources: EU EUDAMED, US FDA

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SMARTSUCTION SOLO DEVICE

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

MPS M ELECTRODE

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

N2000 BASE STATION, N2001 NURSE STATION

FDA 510(k)
FDA Class 2 ·Cardiovascular

UNKNOWN FEMORAL COMPONENT

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 16, 2019

HELICAL BLADE COUPLING SCREW

FDA Adverse Event
Malfunction ·SYNTHES BRANDYWINE·Product code LXH·April 17, 2013

LIGASURE PRECISE

FDA Adverse Event
Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·June 17, 2008

CURLIN ADMINISTRATON SET

FDA Adverse Event
Other ·MOOG MEDICAL DEVICES GROUP·Product code FRN·April 7, 2011

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

CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measured drug therapy to patients in hospital or outpatient settings.

FDA Enforcement
Class II ·Terminated·Smiths Medical ASD, Inc.·June 24, 2015