BEUDAMED
    13 results · 18ms · 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.

    NML-5010/5020 MULTI-DETECTOR SYSTEM

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DD cube ONE ML

    FDA UDI
    Dental Direkt GmbH·EDDIG8320021·DD cube ONE® ML are dental mill blanks made fro...

    ihcDirect® GFAP Ab

    FDA UDI
    NOVODIAX, INC.·00850000596252·Clone R246

    CROWN HOLDING INSTRUMENT

    FDA UDI
    W.H. Holden, Inc.·D9288320020·

    ihcDirect® GFAP Ab

    FDA UDI
    NOVODIAX, INC.·00850000596245·Clone R246

    ihcDirect® GFAP Ab Conjugate 15mL

    FDA UDI
    NOVODIAX, INC.·00850030934468·Clone R246

    ihcDirect® GFAP Ab Conjugate 5mL

    FDA UDI
    NOVODIAX, INC.·00850030934451·Clone R246

    FERTELL FEMALE FERTILITY TEST

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SINGLE USE SOFT TIPPED DISPOSABLE INJECTOR, RAYSERT SINGLE USE SOFT TIPPED SMALL INCISION DISPOSABLE INJECTOR

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    KARL STORZ

    FDA Adverse Event
    Injury ·KARL STORZ ENDOSCOPY·Product code KQT·January 21, 2004

    CORAIL2 ANTERIOR BROACH HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LXH·May 27, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·November 14, 2012

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES·Product code MIH·September 8, 2010