BEUDAMED
    52 results · 16ms · Sources: EU EUDAMED, US FDA

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    Mobile airway scope-diagnosis and observation to access airway anatomy, endotracheal/endobronchial intubation and management. Model Numbers: MAF-DM2, MAF-GM, MAF-GM2, MAF-TM, MAF-TM2.

    FDA Recall
    Open, Classified ·Aizu Olympus Co., Ltd. 3 Chome 1-1 Niiderakita Aizuwakamatsu Japan·Product code EOQ·September 25, 2023

    Olympus Airway Mobilescope, Models MAF-DM2, MAF-GM2, & MAF-TM2.

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code EOQ·July 27, 2023

    Olympus Airway Mobilescope, Models MAF-GM & MAF-TM.

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code EOQ·July 27, 2023

    Airway Mobilescope MAF-TM

    FDA Recall
    Terminated ·Olympus Corporation of the Americas·Product code EOQ·August 8, 2018

    KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco replaces the function of the upper limb on one side of the body.

    FDA Recall
    Open, Classified ·Kinova Inc·Product code IQZ·August 22, 2024

    V-Twin, Catalog # 6002-800, UDI # 03661540600180 Product Usage: automated chemistry analyzer intended for clinical use

    FDA Recall
    Terminated ·Vital Scientific N.V. 24, Kanaalweg Postbus 100 Dieren Netherlands·Product code JJF·January 10, 2012

    COBAS TaqMan analyzer, Series 96; catalog number 8080216.

    FDA Recall
    Terminated ·Roche Molecular Systems Inc·Product code JJF·March 6, 2003

    POWERSAIL Coronary Dilatation Catheter: 3.25x18mm (US) Part #1005524-18

    FDA Recall
    Terminated ·Abbott Vascular-Cardiac Therapies dba Guidant Corporation·Product code MAF·June 17, 2009

    POWERSAIL Coronary Dilatation Catheter: 4.0x8mm (CE) Part #1005726-08

    FDA Recall
    Terminated ·Abbott Vascular-Cardiac Therapies dba Guidant Corporation·Product code MAF·June 17, 2009

    Cytomics FC500 with CXP Software

    FDA Recall
    Terminated ·Beckman Coulter Inc·Product code JJF·November 23, 2005

    Voyager RX Coronary Dilatation Catheter

    FDA Recall
    Terminated ·Guidant Corporation Advanced CardiovascularSystem·Product code MAF·January 27, 2005

    COBAS TaqMan 48 Analyzers.

    FDA Recall
    Terminated ·Roche Molecular Systems Inc·Product code JJF·May 24, 2004

    V-Twin, Model # 6002-800, UDI: 03661540600180 Product Usage: An in-vitro diagnostic device, which is an automated chemistry analyzer, micro type, intended for clinical use in conjunction with certain materials to measure a variety of analytes, including applications in clinical chemistry, monitoring drugs of abuse and in therapeutic drug monitoring.

    FDA Recall
    Open, Classified ·Vital Scientific N.V. 24, Kanaalweg Postbus 100 Dieren Netherlands·Product code JJF·January 18, 2016

    Ormco Damon Q2 Orthodontic Metal Bracket, Part No. 491-9834, L3R Hi Tq Hook, Tq +13 degrees, Rx. Manufactured by Ormco Corporation, This device is intended for use for the orthodontic movement of teeth. It is used temporarily and is removed after orthodontic treatment has been completed.

    FDA Recall
    Terminated ·Ormco/Sybronendo·Product code EJF·January 14, 2020

    Maestro Orthodontic Bracket REF711-298Q QTY. 20 Rx Only (01)00190707017064 (10)889437 (422)484 Maestro Orthodontic Bracket REF711-299MCQ QTY. 20 Rx Only (01)00190707017071(10)889437 (422)484

    FDA Recall
    Terminated ·Ortho Organizers, Inc.·Product code EJF·April 2, 2019

    MULTI-LINK Pixel Coronary Stent System Size: 2.0 x 13 mm OTW Part Number: 1007830-13

    FDA Recall
    Terminated ·Guidant Corporation ACS·Product code MAF·May 7, 2003

    CP STENT (Cheatham Platinum), a prescription device, composed of 90% platinum/10% iridium wire arranged in laser welded rows with a ''zig'' pattern. The number of zigs can be varied and will impact the strength of the stent as well as the eventual diameter and percent stent shortening. CP stents are sold either sterile or non-sterile, and sold in different lengths.

    FDA Recall
    Terminated ·Numed Inc·Product code MAF·June 26, 2003

    BiodivYsio SV Over The Wire (OTW) Coronary Stent, 2.25 mm diameter; Catalog #: B3225-10, Lot #: 010586G; Catalog #: B3225-10, Lot #: 030176G; Catalog #: B3225-15, Lot #: 010626G; Catalog #: B3225-18, Lot #: 020246G.

    FDA Recall
    Terminated ·Abbott Vascular Devices·Product code MAF·July 21, 2003

    The brand name of the device is Damon 3MX Bicuspid Bracket, an orthodontic bracket. Part Number 494-4491, Description -Damon 3MX Bicuspid Bracket, Lot Number - 011265039 Product Usage: Damon 3MX Bicuspid Brackets are intended to be a fixed attachment on a tooth which holds an archwire during orthodontic treatment.

    FDA Recall
    Terminated ·Ormco/Sybronendo·Product code EJF·April 24, 2012

    Avex CX Suite, Avex CX 0.22 UL4,5 HK REF #224-017, Product Usage: Avex CX ceramic brackets are formed with 99.9% pure alumina oxide. The indicated use of the Avex CX ceramic bracket is the mechanical movement of natural teeth in conjunction with other components designed to attach to the brackets.

    FDA Recall
    Terminated ·Ultradent Products, Inc.·Product code EJF·February 8, 2013