BEUDAMED
    28 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 ×

    ORISE ProKnife

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

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694098168·Periosteal Elevator, 3mm Round Edge

    GOLDMAN FOX SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896097445·GOLDMAN FOX SCISSORS STRAIGHT BLADE POWER CUT GOLD

    Histofluor® Rodent LKS Fluorescent Antibody Test System

    FDA UDI
    IMMUNO CONCEPTS INC·M7491200404101·Mouse KS 4 Well Tissue Slides - 10 Slides

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869631587·MOSS VRS head alignment aid, angled

    ASCENDX VCF REDUCTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PC ECG 1200

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWQ·November 23, 2014

    PALL PURECELL REO HIGH EFFICING RAPID FLOW

    FDA Adverse Event
    Injury ·PALL MEDICAL·Product code CAK·May 16, 2005

    PREMIUM PLUS CEEA 25 INSTR. W/TILT-TOP

    FDA Adverse Event
    Injury ·PONCE - USS·Product code GAG·July 27, 2004

    BOSTON SIMPLICITY

    FDA Adverse Event
    Injury ·POLYMER TECHNOLOGY USA·Product code LPN·October 28, 2002

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 28, 2025

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code KFM·July 9, 2024

    CADD-LEGACY PLUS AMBULATORY INFUSION SYSTEM

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·August 8, 2022

    COLLEAGUE 3 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

    VOYAGER NC CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·August 11, 2011

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    DANYANG MAXTHAI MEDICAL EQUIPMENT·Product code IOR·July 1, 2013

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code LKK·April 23, 2012

    Gold Hub Monty Infiltration Cannula, Catalog Nos. IC14HM20; IC16HM15; IC18HM15; IC14HM20; IC16HM15; IC18HM15.

    FDA Recall
    Terminated ·HK Surgical Inc·Product code FIE·December 3, 2004

    Gold Hub Finesse Cannula, Catalog Nos. HK10F23; HK12F10; HK12F15; HK12F23; HK14F10; HK14F15; HK14F23; HK16F5; HK16F8

    FDA Recall
    Terminated ·HK Surgical Inc·Product code FIE·December 3, 2004