BEUDAMED
    8 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.

    MINIM-X 2001-CIAS & MINIM-X 2002-CIAS

    FDA 510(k)
    FDA Class 2 ·Dental

    HEM-O-SCAN OXYGEN EQUIL. CURVE ANALYZER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    GUINEA PIG SERUM - STERILE

    FDA 510(k)
    FDA Class 1 ·Hematology

    COBAS 8000 COBAS C 502 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·April 27, 2026

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·March 12, 2026

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·June 18, 2014

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 26, 2010

    CORAIL AMT COLLAR SIZE 8

    FDA Adverse Event
    Injury ·DEPUY FRANCE S.A.S.-SAINT PRIEST·Product code KWA·December 20, 2012