BEUDAMED
    719 results · 27ms · Sources: EU EUDAMED, US FDA

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    SEATTLE - PAP

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ThermoCool SF NAV

    FDA UDI
    Biosense Webster Inc·10846835009248·

    D-Fine Double Diamond™ Primary Polisher Refill #02

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172001809·Dental burnisher

    ArgenIS

    FDA UDI
    ARGEN CORPORATION, THE·D818131502·MUA NR NP 2.0GH Str

    Batrik Arc Wire Brushes Reusable

    FDA UDI
    Batrik Medical Manufacturing Inc·00690521008106·Brush/White/BD 2mm/BL 15mm/OL 30cm - Flexible -...

    Kirwan (Distributor Gyrus ACMI)

    FDA UDI
    KIRWAN SURGICAL PRODUCTS LLC·00841019108734·Bipolar Iris Forceps, Non-Stick Curved Tips, Re...

    Batrik Arc Wire Brushes Single Use

    FDA UDI
    Batrik Medical Manufacturing Inc·00690521008113·Brush/White/BD 2mm/BL 15mm/OL 30cm - Flexible -...

    n/a

    FDA UDI
    Ortho Development Corporation·00822409067046·Slotted Stem Trial 13x150mm

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857561038·Parallel Trial Size 9x28x7 mm

    USFILTER BICARBONATE MIXING AND DISPENSING (BICARB) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BD VACUTAINER RAPID SERUM TUBE BLOOD COLLECTION TUBE, MODEL 368774

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI PLANT - ST. PAUL·Product code LWS·October 1, 2014

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 14, 2013

    2649622-2003-00087

    FDA Adverse Event
    Injury ·MPRI·June 16, 2011

    Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'

    FDA Enforcement
    Class II ·Ongoing·Molnlycke Health Care, Inc·May 24, 2017

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 30, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 21, 2021

    BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·May 9, 2018

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 24, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 24, 2021