BEUDAMED
    29 results · 22ms · Sources: EU EUDAMED, US FDA

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    SUPER SEAL TOOTH DESENSITIZER

    FDA 510(k)
    FDA Class 2 ·Dental

    Unity Total Knee System

    FDA UDI
    CORIN LTD·05056139243288·UNITY KNEE™ PS-C INSERT - Size 1 x 9mm

    ACRY SMART DIGITAL

    FDA UDI
    DENTAL MANUFACTURING SPA·08056865152417·

    Aztec

    FDA UDI
    Aztecmed/Ent LLC·B87111201090·Klinik Nasal Speculum Infant

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694040372·PrimaLIF LLIF 9mm Box Osteotome

    DURAVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948006773·DURAVENT XL 1 IC, SIZE 9

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319719954·Semken Dressing Forceps 6" (15cm), serrated

    NA

    FDA UDI
    STRYKER CORPORATION·04546540993717·1.5mm Drill Tip

    SIGMA DIAGNOSTICS ACCUCLOT LA CONTROL

    FDA 510(k)
    FDA Class 2 ·Hematology

    LOGIFLEX LAPAROSCOPIC BAND POSITIONING DEVICE

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

    VENTED AUTOFEED CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·April 10, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 12, 2016

    EUROPEAN VALVE SET, EM2400

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·December 10, 2019

    SERIES A PAT STD 31 3 PEG

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·May 20, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 26, 2011

    VICRYL RAPIDE (POLYGLACTIN 910) SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code GAM·August 14, 2008

    VENTED AUTOFEED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·August 1, 2012

    ULTRASONIC GASTROVIDEOSCOPE

    FDA Adverse Event
    Injury ·SHIRAKAWA OLYMPUS CO., LTD.·Product code ODG·January 19, 2023

    EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE

    FDA Adverse Event
    Injury ·SHIRAKAWA OLYMPUS CO., LTD.·Product code ODG·January 19, 2023

    SINGLE USE ASPIRATION NEEDLE NA-U200H

    FDA Adverse Event
    Injury ·OLYMPUS AMERICA, INC·Product code FCG·January 19, 2023