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

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    Filters Regulation: Us FDA ×

    Expandable Titanium PLIF/TLIF System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772344123·PROTECT.PRO ACTION BACK SUPPORT BLACK L

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515235564·Yasargil Bay Fcps, 0.5mm, 8 1/4"

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694019330·Sharp Hook

    24M - Southwest Gas Corp

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588010441·24M - Southwest Gas Corp

    HEMOSIL HIGH ABNORMAL CONTROL ASSAYED

    FDA 510(k)
    FDA Class 2 ·Hematology

    PASS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    466P306X

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DQO·June 29, 2017

    ENDOLOOP LIGATURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GEA·December 28, 2018

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·August 7, 2018

    466P306X

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DQO·June 29, 2017

    SAFETY SYRINGE WITH NEEDLE

    FDA Adverse Event
    Malfunction ·RETRACTABLE TECHNOLOGIES, INC·Product code MEG·August 9, 2021

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·August 27, 2010

    KINAIR MEDSURGE PULSE

    FDA Adverse Event
    Injury ·KCI·Product code IOQ·July 14, 2010

    COLLEAGUE VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE (SG)·Product code FRN·October 20, 2008

    AO LARGE REAMER ATTACHMENT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·July 1, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 2, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·August 27, 2010

    ENDOPATH*STEALTH CIR STAPLER (EXACT CODE UNKNOWN)

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·December 26, 2018

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·August 31, 2010