BEUDAMED
    40 results · 23ms · Sources: EU EUDAMED, US FDA

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    D-STAT DRY SILVER; D-STAT DRY CLEAR SILVER; D-STAT DRY WRAP SILVER; THROMBIX SILVER

    FDA 510(k)
    FDA Unclassified ·Unknown

    GoLIF! Lumbar Interbody Fusion System

    FDA UDI
    GetSet Surgical SA·07640387660317·GoLIF! Lumbar Interbody Fusion Device, 1 PEEK p...

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814657·GENUMEDI SILVER SIZE II

    DURAVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948005509·DURAVENT UNI 1 IC + 1 ICU, SIZE 12

    JOBST Bella Strong

    FDA UDI
    BSN MEDICAL, INC.·00035664008482·BELLA STRONG 15-20 MM HG ARMSLEEVE DOT BAND SIZ...

    REPICCI II RESURFACING KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304446991·

    CRYOPEN CRYOSURGICAL SYSTEM, K102214

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

    MODIFICATION TO AEQUALIS SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MIRAGE HYDROPHILIC GUIDEWIRE, MODEL 103-0608

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LUX Expandable Interbody System

    FDA UDI
    XENIX MEDICAL LLC·00840493416038·Lumbar Expandable, 10x22x12-16mm, 15 Deg

    Plateau Spacer System

    FDA UDI
    Life Spine, Inc.·00190837026097·PLATEAU Interbody, Straight, Bulleted, 10mm 22m...

    LUX Expandable Interbody System

    FDA UDI
    XENIX MEDICAL LLC·00840493416021·Lumbar Expandable, 10x22x12-16mm, 8 Deg

    MOSAIC MITRAL BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·August 2, 2019

    CG FUTURE BAND

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·October 15, 2018

    Epiphany

    FDA UDI
    PANTHEON SPINAL, LLC·B528100310021022120·Curved Osteotome Shaft 10mm

    OT ULTRAMINI METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 9, 2013

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code MTA·September 19, 2014

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·May 19, 2011

    Fortilink Cages with TiPlus Technology

    FDA UDI
    Baat Medical Products B.V.·08720246785197·

    Fortilink Cages with TiPlus Technology

    FDA UDI
    Baat Medical Products B.V.·08720246785098·