BEUDAMED
    23 results · 23ms · 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 ×

    PASTEUR PIPET - STERILE 9, PASTEUR PIPET - STERILE 5 3/4, MODELS 16-PP-9, 16-PP-5.75

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Essential Kit

    FDA UDI
    MEDIVATORS INC.·40677964008106·Essential Kit includes DEFENDO Valves, Basin, B...

    Immunalysis

    FDA UDI
    IMMUNALYSIS CORP·00840937108307·Opiates Urine Calibrator 2000, 3

    Synergy Disc Instruments

    FDA UDI
    Synergy Spine Solutions Inc·M67091000009150·Trial, Small, 5mm, 0°

    TELSTAR BIPLANE DIGITAL IMAGING SYSTEM [TIS] MODEL 030-000915

    FDA 510(k)
    FDA Class 2 ·Radiology

    BARCOMED 2MP2

    FDA 510(k)
    FDA Class 2 ·Radiology

    RETIC CHEX LINEARITY

    FDA 510(k)
    FDA Class 2 ·Hematology

    SECURE FLOW

    FDA Adverse Event
    Injury ·WOO YOUNG MEDICAL INC.·Product code MEB·March 27, 2012

    EliteCore Full Core Biopsy Device. EliteCore 18G, 20cm with and without HiLiter tip, 15 cm with and without HiLiter tip, and 10 cm with and without HiLiter tip.

    FDA Enforcement
    Class II ·Terminated·Stryker Instruments Div. of Stryker Corporation·June 3, 2015

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 13, 2013

    UNKNOWN ZIMMER MIS TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·February 18, 2011

    LADARVISION

    FDA Adverse Event
    Injury ·ALCON - ORLANDO TECHNOLOGY CENTER·Product code LZS·February 20, 2008

    L3W0750 - DUODERM

    FDA Adverse Event
    Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code NAD·February 17, 2022

    DUODERM

    FDA Adverse Event
    Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code NAD·October 3, 2022

    DUODERM/GRANUFLEX/DUOACTIVE - MOISTURE RETENTIVE DUODERM CGF DRESSING

    FDA Adverse Event
    Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code NAD·August 6, 2018

    VERCISE GENUS?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code MHY·February 24, 2026

    L3W0750 - DUODERM

    FDA Adverse Event
    Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code NAD·May 25, 2021

    L3W0750 - DUODERM

    FDA Adverse Event
    Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code NAD·December 22, 2020

    DUODERM

    FDA Adverse Event
    Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code NAD·June 7, 2023

    DUODERM

    FDA Adverse Event
    Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code NAD·May 9, 2025