9 results · 19ms · Sources: EU EUDAMED, US FDA

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SERIES 1500 RESPONDER

FDA 510(k)
FDA Class 2 ·Cardiovascular

NA

FDA UDI
Zimmer, Inc.·00889024156593·

INJECTOR LUER, MODEL N34, INJECTOR LUER LOCK, MODEL N35, INJECTOR LUER LOCK, N35C, CONNECTOR LUER LOCK, MODEL C35,

FDA 510(k)
FDA Class 2 ·General Hospital

HERMES HD AQ ACQUISITION STATION AND HERMES WORKSTATION

FDA 510(k)
FDA Class 2 ·Radiology

OT PING ENHANCED METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013

INFINITI VISION SYSTEM OZIL

FDA Adverse Event
Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·February 14, 2014

CAPSUREFIX NOVUS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·November 18, 2010

CAP FOR INJECTOR MEMBRANE M50

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·May 4, 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