BEUDAMED
    43 results · 20ms · Sources: EU EUDAMED, US FDA

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    24M - Memphis Light & Gas - Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588000077·24M - Memphis Light & Gas - Metal

    PROFEMUR GLADIATOR Thin HA Classic Hip Stem with Collar

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Paradigm

    FDA UDI
    Proprio, Inc.·00850042604038·Paradigm Surgical Instrument Tray

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377046901·RELINE-O Trial, 11mm H Lamina N L-pop

    Zavation

    FDA UDI
    Zavation LLC·00842166131552·Ti3Z CIF 12mmx14mmx7mm -0 deg

    MicroAire®

    FDA UDI
    Microaire Surgical Instruments LLC·00847399000866·SMALL SAGITTAL SAW BLADE, 4.3mm X 15mm X 0.5mm

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694005616·1.6mm Pilot Drill, Manual

    iNAP

    FDA UDI
    SOMNICS, INC.·04719878320115·iNAP Saliva Container

    JEWELERS PRECISION FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896059351·JEWELERS PRECISION FORCEPS #PP SERRATED HANDLE

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·HeartSync Multifunction Disposable Single-Use AED Defibrillator Pads

    SAFYRE SLING SYSTEM

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

    IMMULITE CARBAMAZEPINE, IMMULITE 2000 CARBAMAZEPINE, CATALOG # LKCB1, LKCB5 & L2KCB2, L2KCB6

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·HeartSync Multifunction Disposable Single-Use AED Defibrillator Pads

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·HeartSync Multifunction Disposable Single-Use Defibrillator Pads

    PHYSICA KR LINER

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A·Product code MBH·December 20, 2022

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·June 9, 2017

    SPRINT

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 9, 2017

    SMR HUMERAL HEAD DIA. 46MM

    FDA Adverse Event
    Other ·LIMACORPORATE S.P.A.·Product code KWT·March 5, 2014

    AUTO SUTURE TA PREMIUM 55

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL CORPORATION·Product code GAG·August 10, 2000

    BINAXNOW¿ COVID-19 AG CARD

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·January 4, 2022