BEUDAMED
    41 results · 21ms · Sources: EU EUDAMED, US FDA

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    RGP MULTI-PURPOSE SOLUTION ID 100136

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741028823·Catheter Placement Kit

    Truflex™

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730011947·Truflex™ PT SE NiTi Upper 21x25 38mm 10/PK

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014602820·Schure Strap Brand Rolls, 1.5"W

    ESU Shroud

    FDA UDI
    I.C. MEDICAL, INC.·00817688021070·

    LIFEPAK® CR Plus and LIFEPAK Express defibrillators

    FDA UDI
    PHYSIO-CONTROL, INC.·00885074440132·PACKAGE,LPCR PLUS,SEMI,ENGLISH,AHA2005

    LIFEPAK CR Plus and LIFEPAK Express defibrillators

    FDA UDI
    PHYSIO-CONTROL, INC.·00883873820506·PACKAGE,LPCR PLUS,SEMI,ENGLISH,AHA2005, FDA

    LISO2,FAA,LITHIUM BATTERY

    FDA UDI
    PHYSIO-CONTROL, INC.·00883873981641·KIT-LISO2,FAA,LITHIUM BATTERY REPLACEMENT ASSY

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 18, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 18, 2025

    SEALOUETTE FIBRIN SEALANT EXTENDED DROPLET APPLICATOR, MODEL TE-1

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RAPID RHINO-ANTERIOR 90MM, MODEL RR-A 90, RAPID RHINO-POSTERIOR 100MM, MODEL RR-P 100

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    Quantum

    FDA UDI
    SPECTRUM MEDICAL LIMITED·05060434423726·Quantum Flow Sensor - ID1/8" x Wall 1/16" (OD1/...

    Thermodilution Catheter and Accessories

    FDA UDI
    BIOPTIMAL INTERNATIONAL PTE. LTD.·08886483501355·

    Thermodilution Catheter and Accessories

    FDA UDI
    BIOPTIMAL INTERNATIONAL PTE. LTD.·00886333222223·

    SERIES 7000 STANDARD TIBIA

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·August 29, 2012

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·April 3, 2025

    WALLACH ULTRA FREEZE

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·August 23, 2021

    RUSCH AGT NASAL PERFORMED ET TUBE, 7.0MM

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BSK·March 8, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·February 24, 2011