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

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    Hydrofera Blue READY - Border

    FDA 510(k)
    FDA Unclassified ·Unknown

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017880·K-Wire, Double Ended, Trocar Point, Diameter Si...

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306804465·Robotti Micro Elevator, 2mm, Length: 16 cm / 6....

    SYRINGE 50ML LL BNS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·January 30, 2025

    SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SHIMADZU MOBILE X-RAY SYSTEM MOBILE ART EVOLUTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    ONE TOUCH PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·January 6, 2003

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 19, 2022

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OYC·February 11, 2019

    BD SOLOMED SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·February 11, 2021

    RENASYS GO RENTAL DEVICE

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code OMP·October 21, 2014

    CURLIN IV PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVIECS GROUP·Product code FRN·June 10, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·July 19, 2011

    SYRINGE 50ML LL BNS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·January 30, 2025

    BD SYRINGE SOLOMED 3ML LL 22X1-1/4 W/SH SLA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·December 17, 2019

    Ulrich medical neon3 OCT spinal stabilization, REF CS 3917-12, Locking screw for crosslink, screw-to-screw

    FDA Recall
    Terminated ·ulrich medical USA Inc·Product code KWP·December 31, 2019

    ULRICH Torque Limiting Handle for use with a Set Screw Driver to perform the final tightening of set screws in a spinal implant construct.

    FDA Recall
    Terminated ·ulrich medical USA Inc·Product code LXL·March 8, 2019

    Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026

    Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026