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

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    BIOPHOTAS CELLUMA

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Anterolateral Tibia Plate

    FDA UDI
    I.T.S. GmbH·09120047299791·Anterolateral Tibia Plate, 13-Hole, Right

    CATHETER MOUNT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZO·October 24, 2014

    GUARDIAN II NC HEMOSTASIS VALVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DISPOSABLE POWDER FREE VINYL EXAM GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523184095·L CR E-CIMA Vitamin E Congruent Tibial Insert S...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523184330·L CR Tibial Insert Trial Sz A 13mm

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005118·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005132·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005125·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005163·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005149·CONTINUOUS SUCTION REGULATORS

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072005156·CONTINUOUS SUCTION REGULATORS

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 1, 2014

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH LTD/HUNTINGTON·Product code HQL·May 23, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011

    ADULT DUAL HEATED EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·April 17, 2014

    Conical portio adapter (acorn) small & large are used for examination and diagnosis in conjunction with endoscopic accessories in gynecological laparoscopy, to determine patency of the fallopian tubes.

    FDA Recall
    Terminated ·Richard Wolf Medical Instruments Corp.·Product code HHI·May 19, 2016

    cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V

    FDA Enforcement
    Class II ·Terminated·Roche Diagnostics Corporation·March 14, 2018