BEUDAMED
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    DORO® NON-STICK Bipolar Forceps

    FDA UDI
    pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung·04250435505762·DORO® NON-STICK Bipolar Forceps, Bayone...

    DORO® Reusable Skull Pins

    FDA UDI
    pro med instruments GmbH, Herstellung und Vertrieb medizinisch technischer Ausrüstung·04250435508435·DORO® Reusable Skull Pin Titanium, Pediat...

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation

    FDA Pre-Market Approval
    FDA Class 3 ·Arctic Front Advance and Arctic Front Advance Pro

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation

    FDA Pre-Market Approval
    FDA Class 3 ·Arctic Front Advance and Arctic Front Advance Pro

    Aortic Valve, Prosthesis, Percutaneously Delivered

    FDA Pre-Market Approval
    FDA Class 3 ·CoreValve TAV, Evolut-R TAV, Evolut PRO TAV

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX

    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·USCI(R)SOLITAIRE(TM) BALL.DIL.CATH.W/PRO/PEL(TM)

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation

    FDA Pre-Market Approval
    FDA Class 3 ·Arctic Front Advance and Arctic Front Advance Pro

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation

    FDA Pre-Market Approval
    FDA Class 3 ·Arctic Front Advance and Arctic Front Advance Pro

    Calcium Salt Bone Void Filler, Drillable, Non-Screw Augmentation

    FDA Pre-Market Approval
    FDA Class 2 ·PRO OSTEON IMPLANT 500 HYDROXYAPATITE BONE VOID FILLER

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation

    FDA Pre-Market Approval
    FDA Class 3 ·Arctic Front Advance and Arctic Front Advance Pro

    Heart-Valve, Non-Allograft Tissue

    FDA Pre-Market Approval
    FDA Class 3 ·Medtronic CoreValve Evolut PRO TAV, and Avalus Bioprosthesis

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX

    Prime Screen

    FDA UDI
    WONDFO USA CO., LTD.·00816862024166·Prime Screen® Multi-Drug Urine Test Cup, 14-Pan...

    UScreen®

    FDA UDI
    Instant Technologies, Inc.·00817405021178·U-Screen Squared Integrated CLIA Waived Cup wit...

    Alere iCup Dx

    FDA UDI
    Instant Technologies, Inc.·00817405020348·Drugs of Abuse Test Cup for detection of BZO+BA...

    U-Screen

    FDA UDI
    Instant Tech Subsidiary Acquisition·00858998006135·U-Screen Squared Integrated CLIA Waived Cup wit...

    U-Screen

    FDA UDI
    Instant Tech Subsidiary Acquisition·00858998006111·U-Screen Squared Integrated CLIA Waived Cup wit...

    Identify Diagnostics Drug Test Cups

    FDA UDI
    UCP BIOSCIENCES, INC.·10817038021689·Identify Diagnostics Drug Test Cups 12-Panel Dr...