BEUDAMED
    18 results · 37ms · Sources: EU EUDAMED, US FDA

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    TSH ENZYME IMMUNOASSAY TEST KIT CAT. NO. KIF4093

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111000·INSTRUMENT CADDY SMALL

    ULTHERA SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ANIMUS EZSERTER INFUSION SET INSERTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TAP F/CORTSCR Ø3.5 L110/50

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code HWX·January 18, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·February 6, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·December 13, 2010

    BOWER RING PEG SYSTEM

    FDA Adverse Event
    Injury ·CORPAK, INC.·Product code EZL·November 3, 1992

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    UNKNOWN IMPACTOR

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HWA·April 12, 2021

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026