BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    Lelo Hex Natural Rubber Latex Condom

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ABC

    FDA UDI
    Conmed Corporation·10653405003861·ABC PROBE 5 MM HANDSWITCHING PROBE, 44 CM

    HAMILTON MEDICAL AG

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·June 19, 2023

    OPTOS LIMITED PANORAMIC 200CAF

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    AHMED GLAUCOMA VALVE, MODEL M4

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·July 7, 2011

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    UNKNOWN·Product code ITJ·June 10, 2013

    CENTRICITY RA1000

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE INTEGRATED IT SOLUTIONS·Product code LLZ·September 1, 2008

    AMISTEM H FEMORAL CEMENTLESS STEM SIZE 5 STD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 1, 2017

    ABC PROBE REF 160644 5 mm Handswitching Probe, 44 cm QTY: 1 STERILE CONMED CORPORATION 525 French Rd, Utica, NY 13502... ASSEMBLED IN MEXICO ABC PROBE REF 160636 5 mm Handswitching Probe, 44 cm QTY: 10 STERILE CONMED CORPORATION 525 FRENCH RD UTICA, NY 13502 ASSEMBLED IN MEXICO Usage: Electrosurgical handpiece for use as monopolar electrosurgical accessory in conjunction with CONMED electrosurgical units equipped with argon beam coagulation.

    FDA Recall
    Terminated ·ConMed Electrosurgery·Product code GEI·December 18, 2008