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

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    Medical surgical mask

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Fluid Retention Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112854·VIDAURRI FLUID RETENTION WELL 8.7MM

    Conventional Lead Apron .5mm Xtra Xtra Large 26 X 42

    FDA UDI
    Flow X Ray Corporation·00843696123925·Conventional Lead Apron .5mm XXL 26 X 42, Elect...

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112786·BARRON VACUUM PUNCH 8.25MM

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112946·CORNEAL TREPHINE BLADE8.25MM

    HIP TOOL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ETEST LINEZOLID

    FDA 510(k)
    FDA Class 2 ·Microbiology

    BERLIN HEART EXCOR DRIVING TUBE, BLUE

    FDA Adverse Event
    Malfunction ·BERLIN HEART GMBH·Product code DSQ·November 9, 2021

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 13, 2024

    UNKNOWN COOL TIP ELECRTRODE

    FDA Adverse Event
    Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·January 27, 2022

    UNKNOWN EMPRINT ANTENNA

    FDA Adverse Event
    Injury ·COVIDIEN LP - SUPERDIMENSION INC·Product code NEY·June 17, 2021

    SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·October 16, 2008

    RAT TOOTH FORCEPS

    FDA Adverse Event
    Injury ·COOK UROLOGICAL, INC.·Product code FAD·August 5, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013

    REZUM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 6, 2024

    BREATHING CIRCUIT SET

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code BZO·May 28, 2026

    MAGNETOM Vida Fit. Model Number: 11410481.

    FDA Enforcement
    Class I ·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025

    PROTEGE RX CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NIM·August 19, 2021

    SPIDER FX

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NTE·August 19, 2021

    POWERPICC SOLO2 CATHETER BASIC TRAY (4F) (SINGLE-LUMEN)

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code LJS·June 3, 2021