BEUDAMED
    23 results · 20ms · 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.

    SALINE IV FLUSH SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092002142·artVeneer life upper posteriors, L, D3

    SCANLAN®

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159018189·Vascular Clamp Straight Jaw

    Metal Custom Rx

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746102486·BRACKET SINGLE WIDTH 022 TQ=0 A=0 R=0 PROFILE=S...

    CURE OPEL-L (S)

    FDA UDI
    MEDITECH SPINE, LLC·B167900021420·

    OPEL-L

    FDA UDI
    SpineArt SA·07640332477205·OPEL-L PLATE ASSEMBLY, L42

    CURE OPEL-L (S)

    FDA UDI
    MEDITECH SPINE, LLC·B167S1900021420·

    AUDIO TECHNOLOGIES S:R.1

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    MIDAS TOUCH LATEX EXAMINATION GLOVES-POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    16PW - Norfolk Southern 002142-0 - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588170077·16PW - Norfolk Southern 002142-0 - Poly White

    Z.S.G.M. CUTTER 2:1 RATIO ( CAUTION: SHARP )

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·August 28, 2023

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·February 11, 2013

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 18, 2011

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN - BENNETT CORP.·Product code CBK·February 25, 2008

    TRULIANT PS CEM FEM PS CEM RIGHT SZ 6

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 12, 2023

    VOYANT® FINE FUSION DEVICE

    FDA Adverse Event
    Injury ·APPLIED MEDICAL RESOURCES·Product code GEI·August 29, 2024

    VOYANT® FINE FUSION DEVICE

    FDA Adverse Event
    Injury ·APPLIED MEDICAL RESOURCES·Product code GEI·August 29, 2024

    VOYANT® FINE FUSION DEVICE

    FDA Adverse Event
    Injury ·APPLIED MEDICAL RESOURCES·Product code GEI·August 29, 2024

    VOYANT® FINE FUSION DEVICE

    FDA Adverse Event
    Injury ·APPLIED MEDICAL RESOURCES·Product code GEI·August 29, 2024

    Smiths Medical, Medfusion¿ Syringe Infusion Pump, Model 4000, Software Version V1.0 & V1.1, Reorder Numbers 4000-0100-50, 4000-0100-95, 4000-0101-50, 4000-0101-51, and 4000-0101-78. Designed for use in care areas for the administration of fluids requiring precisely controlled infusion rates.

    FDA Enforcement
    Class I ·Terminated·Smiths Medical ASD, Inc.·August 8, 2012