BEUDAMED
    110 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Terminated ×

    BBL Columbia C.N.A. Agar w/5% Sheep Blood - Catalog Number 297831.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    Sheep Blood, Defibrinated - Catalog Number 212390, Unit 60 ml.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    Sheep Blood, Defibrinated - Catalog Number 211947, Unit 500 ml.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    BBL TSA II w/5% Sheep Blood, Spacesaver - Catalog Number 292537.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    Sheep Blood, Defibrinated - Catalog Number 212389, Unit 30 ml.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    Sheep Blood, Defibrinated - Catalog Number 212391, Unit 250 ml.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    Sheep Blood, Defibrinated - Catalog Number 211945, Unit 15 ml.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    Sheep Blood, Defibrinated - Catalog Number 211946, Unit 100 ml.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    BBL Columbia C.N.A. Agar w/5% Sheep Blood/Levine EMB - Catalog Number 295618.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    BBL Brain Heart Infusion Agar CC w/Sheep Blood - Catalog Number 296178.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    BBL Brain Heart Infusion Agar w/10% Sheep Blood - Catalog Number 297655.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    AVI Sterile Impad Rigid Sole Foot Cover, Right Foot Product Code:6066

    FDA Recall
    Terminated ·Product code JOW·August 11, 2010

    AVI Sterile Impad Rigid Sole Foot Cover, Left Foot Product Code:6067

    FDA Recall
    Terminated ·Product code JOW·August 11, 2010

    Symmetry Olsen monopolar cord: (a) Monopolar Cord, 1/8" Diameter Pin, TUR Connector, 10' (3.0m), REF 92002, QTY 50 (b) Monopolar Cord, Bovie to 90o Female Pin, 10' (3.0m), REF 40-2106, QTY 10 (c) Monopolar Cord, Bovie to 90o Female Pin, 10' (3.0m), REF 40-2110, QTY 10 Designed to bring high frequency electrical power from the electrosurgical generator to the active.

    FDA Recall
    Terminated ·Olsen Medical·Product code GEI·May 11, 2018

    Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.

    FDA Enforcement
    Class II ·Terminated·Mizuho OSI·February 20, 2013

    Mizuho OSI Trios, Table Base; Voltage: 100-240V ~ 50/60 Hz Amps: 5,0-5.0A; Model 7803 and 7803AP Orthopaedic: Operating room tablebase - an electronically powered mobile operating table is created, designed for temporary (<24 hours) support and positioning of a patient in a prone, supine, or lateral position depending on the specific table top utilized.

    FDA Enforcement
    Class II ·Terminated·Mizuho OSI·February 17, 2016

    216 Wilson Frame Pads, Model # 5319-37; Used with Radiolucent Wilson Frames, model numbers 5319G and 5321G. General and Plastic Surgery: These pads are used as a component of the Wilson Frames, which support the torso of a prone patient during spine surgery. The pads are supplied with the frames and as replacements.

    FDA Enforcement
    Class II ·Terminated·Mizuho OSI·April 26, 2017

    Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI - Product Usage: used with Mizuho OSI spinal surgery tables to provide patient head support and positioning during spinal surgery.

    FDA Enforcement
    Class II ·Terminated·Mizuho OSI·October 21, 2020

    CDLCAM, First-Pass Radionuclide Angiography Camera System, Model 70-500101, with operating Software Version B1A, marketed by CDL Medical Tech.

    FDA Recall
    Terminated ·GVI Technology Partners·Product code IYX·January 16, 2004

    BVX-450NR Bovie Precise 360 Handpiece 45cm, needle Product is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures.

    FDA Recall
    Terminated ·Bovie Medical Corporation·Product code GEI·July 18, 2016