BEUDAMED
    29 results · 25ms · 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 Regulation: Us FDA ×

    MIS Dental Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    Tether

    FDA UDI
    Seaspine Orthopedics Corporation·10889981101602·Fixed Angle Center Guide

    DEBAKEY TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896059764·DEBAKEY TISSUE FORCEPS FLAT HANDLE

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694010962·Bone Clamp

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR32001021·Distance ring 2 mm f. mand. protrusion appliance

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869608237·TELIX K Impact Cap

    BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·June 21, 2023

    BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·July 20, 2023

    GLUCOSE (HEXOKINASE) LIQUID REAGENT, MODEL G518-150

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    IQTEQ SPIROMETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BD VACUTAINER® K2 EDTA BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·July 20, 2023

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDO·May 3, 2001

    SYSTEM 1000 SPDS

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code FKP·October 8, 2003

    MODEL EMV+ VENT, ARMY, COMMERCIAL

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code CBK·January 3, 2025

    PRECISION LINK

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·October 15, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 1, 2013

    CADD LEGACY 1 PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·June 9, 2022

    MEDTRONIC TRANSCATHETER VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·June 17, 2022

    ZYPLAST COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·COLLAGEN CORP.·Product code LMH·January 14, 1999