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HARBOR MEDICAL INC.

FDA registration
HARBOR MEDICAL INC.·2 products·🇺🇸 United States

HYGIENE SLING

FDA Adverse Event
Injury ·HARBOR MEDICAL, INC·Product code FSA·April 7, 2008

SEAPORT IMPLANTABLE DEVICES

FDA Adverse Event
Injury ·HARBOR MEDICAL DEVICES, INC·Product code LKG·July 23, 1992

SEAPORT IMPLANTABLE DEVICES

FDA Adverse Event
Injury ·HARBOR MEDICAL DEVICES, INC.·Product code LKG·July 23, 1992

INTROCAN SAFETY

FDA Adverse Event
Malfunction ·B. BRAUN MELSUNGEN AG·Product code FOZ·June 7, 2021

BEKA HOSPITEC SLING LIFT CARLO

FDA Adverse Event
Death ·BEKA HOSPITEC / HARBOR MEDICAL INC.·Product code FSA·May 17, 2019

INQUIRY ¿ STEERABLE DIAGNOSTIC CATHETER

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC.·Product code DRF·May 22, 2023

MEDTRONIC NAVIGATION

FDA Adverse Event
Injury ·MEDTRONIC NAVIGATION, INC·Product code GEX·February 24, 2021

MCKESSON POLYGLYCOLIC ACID 5-0

FDA Adverse Event
Injury ·COVIDIEN·Product code GAM·September 24, 2025

Winged Infusion Set with 90 degree Huber Needle and Y Injection Site Distributed By: FloridaInfustion Services, Inc., Palm Harbor, FL 34683 Item # FIY-2210 Intended use: Intravascular Administration Set

FDA Recall
Terminated ·Churchill Medical Systems, Inc.·Product code FPA·November 16, 2010

syngo Dynamics version 9.0, Siemens Medical Solutions, USA, Inc., Ann Arbor, MI. The syngo Dynamics is a picture archiving and communications system intended for acceptance, transfer, display, storage, archiving and manipulation of digital medical images, including quantification and report generation. It is not intended to be used for the reading of mammography images.

FDA Recall
Terminated ·Siemens Medical Solutions, USA, Inc·Product code LLZ·March 24, 2011

Custom Sheath Introducer Kit REF K21-00031 - Product Usage: intended use is to provide access and facilitate the percutaneous introduction of various devices into vein.

FDA Recall
Terminated ·Merit Medical Systems, Inc.·Product code DYB·September 12, 2019

Radial Assist RAD BOARD, used to support the weight of a patient's arm and supplies for a medical procedure. The Merit RAD BOARD is a rigid and stiff body board intended for use for various medical purposes. RAD BOARD was specifically designed to support the weight of a patient's arm and supplies for medical procedure, in order to have optimal access to upper extremity vasculature, including radial and brachial arterial and venous access. The RAD BOARD is partially lined with a layer of lead-free Xenolite TB for additional radiation scatter protection.

FDA Recall
Terminated ·Merit Medical Systems, Inc.·Product code BWN·December 18, 2013

MedEnvoy Global BV

Authorized representative
🇳🇱 Netherlands·143 Manufacturers·2306 Devices