BEUDAMED
    11 results · 21ms · 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.
    Filters Regulation: Us FDA ×

    SMARTSITE ACCESS PIN

    FDA 510(k)
    FDA Class 2 ·General Hospital

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970485·anteriors; shade BL1; mould UCS

    SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295250777·SIGMA TIBIAL INSERT FIXED BEARING CURVED PLUS 6...

    BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58L

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AMYLOCHROME STAT SEPARATOR, TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SYNCHRON URIC ACID

    FDA Adverse Event
    BECKMAN COULTER INC.·Product code KNK·June 10, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 20, 2013

    MENISCAL APPLIER

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code HRX·January 20, 2011

    PDS II (POLYDIOXANONE) SUTURE

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·July 31, 2014

    PFC SIGMA MOD TIB TRAY CEM SZ2

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 13, 2022

    SIGMA XLK CVD+ INS 1.5 8MM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 13, 2022