BEUDAMED
    24 results · 23ms · Sources: EU EUDAMED, US FDA

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    Diros OWL Sterile Single Use TridentTM R.F. Insulated Cannulae,Models DTR and DTRH

    FDA 510(k)
    FDA Class 2 ·Neurology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699533·GENUMEDI PSS BLUE, SIZE I

    Oticon

    FDA UDI
    Oticon A/S·05707131287021·H11V2, RITE 312 WL CNB

    OSS™ Orthopedic Salvage System

    FDA UDI
    Biomet Orthopedics, LLC·00880304238992·

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100196·MCINTYRE SPECULUM OPEN WIRE

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962104330·RAPIDCUT BLADE, 3.5MM, COMPATIBLE W/SN

    SPY INTRA-OPERATIVE IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962102343·DISPOSABLE ARTHROSCOPIC 3.5mm RAPIDCUT SHAVER B...

    FREESTYLE PRECISION NEO

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code NBW·January 10, 2017

    PARADIGM QUICKSERTER

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 7, 2014

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 6, 2013

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·June 7, 2011

    UNKNOWN JOINT REPAIR DEV

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026

    UNKNOWN JOINT REPAIR DEVICE

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026

    UNKN JOINT REPAIR DEV

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026

    UNKNOWN

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026

    HEARTMATE 3 SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·October 16, 2022

    UNKNOWN JOINT REPAIR DEV

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026

    UNKNOWN JOINT REPAIR DEVICE

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 6, 2026