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

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    Absorbable Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·ABSORB GT1 BIORESORBABLE VASCULAR SCAFFOLD (BVS) SYSTEM

    Absorbable Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·Absorb GT1 Bioresorbable Vascular Scaffold (BVS) System

    Absorbable Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·Absorb GT1 Bioresorbable Vascular Scaffold (BVS) System.

    Absorbable Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·ABSORB GT1 BIORESORBABLE VASCULAR SCAFFOLD (BVS) SYSTEM

    Absorbable Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·ABSORB GT1 BIORESORBABLE VASCULAR SCAFFOLD (BVS) SYSTEM

    Absorbable Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·ABSORB GT1 BIORESORBABLE VASCULAR SCAFFOLD (BVS) SYSTEM

    Absorbable Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·Absorb GT1 Bioresorbable Vascular Scaffold (BVS) System

    Absorbable Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·ABSORB GT1 BIORESORBABLE VASCULAR SCAFFOLD (BVS) SYSTEM

    Absorbable Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·ABSORB GT1 BIORESORBABLE VASCULAR SCAFFOLD (BVS) SYSTEM

    Absorbable Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·Absorb GTi Bioresorbable Vascular Scaffold (BVS) System

    PRO ADVANTAGE

    FDA UDI
    NATIONAL DISTRIBUTION & CONTRACTING, INC.·M220P7500233·PRO ADVANTAGE EXAM TPT 30X42 WHITE 50/CS

    TMA - Archwire

    FDA UDI
    ORMCO CORPORATION·00889989029451·TMA REV.CURVE/LOOPS 016X022 34MM PK/5

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776207878·FLEIBLE GRASPER ALIGATOR FCP Long

    MIRABAY

    FDA UDI
    Mirabay Orthodontics Corp.·05061075022538·KLEOS PSL METAL ROTH 022 LR5 HK PK5

    OptiMesh Multiplanar Expandable Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7403150023·Powered Straight Brush

    Q-Rejuvalight Pro Facewear (Model: P19-0023)

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

    HEARTLIGHT

    FDA Adverse Event
    Injury ·CARDIOFOCUS·Product code OAE·November 26, 2018

    Vertessa Lite Y-Mesh

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

    EVERFLEX SELF-EXPANDING PERIPHERAL STENT WITH ENTRUST DELIVERY SYSTEM LONG

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code NIP·March 9, 2016

    EVERFLEX SELF-EXPANDING PERIPHERAL STENT WITH ENTRUST DELIVERY SYSTEM LONG

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code NIP·March 9, 2016