BEUDAMED
    30 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.
    Filters Regulation: Us FDA ×

    NeuroQ 3.8

    FDA 510(k)
    FDA Class 2 ·Radiology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694053556·NeuroPack, Profile 0, 2 straight plates, 4 Auto...

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010395·PedFuse Reset, SLD, 8.0mm x 80mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010326·PedFuse Reset, SLD, 8.0mm x 45mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010388·PedFuse Reset, SLD, 8.0mm x 75mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010340·PedFuse Reset, SLD, 8.0mm x 55mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010319·PedFuse Reset, SLD, 8.0mm x 40mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010333·PedFuse Reset, SLD, 8.0mm x 50mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010371·PedFuse Reset, SLD, 8.0mm x 70mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010302·PedFuse Reset, SLD, 8.0mm x 35mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010296·PedFuse Reset, SLD, 8.0mm x 30mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010364·PedFuse Reset, SLD, 8.0mm x 65mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010357·PedFuse Reset, SLD, 8.0mm x 60mm

    CLAVE STOPCOCK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NELLCOR COMPATIBLE REUSABLE SPO2 SOFT-FINGER SENSOR, MODEL T100A-090103

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD BACTEC¿ MGIT¿ 960 SUPPLEMENT KIT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·February 4, 2025

    DORMA 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·March 16, 2022

    SROM STM STD 36+12L 13X18

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code JDI·October 25, 2017

    INSTINCT ENDOSCOPIC HEMOCLIP

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL, INC.·Product code MND·June 13, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011