BEUDAMED
    9 results · 22ms · 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.

    GEN-PROBE ACCUPROBE GROUP B STREPTOCOCCUS CULTURE IDENTIFICATION TEST 2820

    FDA 510(k)
    FDA Class 1 ·Microbiology

    EMDS GLUCOSE (GLU-HK) TEST, ITEM 65415

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ALLEGRO (TM) FERRITIN IMMUNOASSAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    TRIDENT 0° INSERT TRIAL 36MM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·March 31, 2025

    ENDOPATH THORACIC ENDO LINEAR CUTTER WITH SAFETY LOCK

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·August 20, 1997

    ENDOPATH THORACIC ENDO LINEAR CUTTER WITH SAFETY LOCK

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·August 20, 1997