BEUDAMED
    8 results · 20ms · 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.

    GM60A-32S, GM60A-40S

    FDA 510(k)
    FDA Class 2 ·Radiology

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111451683·PEAN NIPPON HEMO FCP STR 7 INCHES

    HAND STC, MODEL 60MM

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

    P200MAAF

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    GMK-SPHERE 02.12.0310FL TIBIAL INSERT FIXED SPHERE FLEX SIZE 3/10 MM L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 8, 2022

    OT ULTRALINK METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 6, 2014

    EYE SURGERY STRETCHER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·June 3, 2013

    LENSTAR LS 900

    FDA Adverse Event
    Injury ·HAAG-STREIT AG·Product code HJO·June 21, 2011