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

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    Catheters, Transluminal Coronary Angioplasty, Percutaneous

    FDA Pre-Market Approval
    FDA Class 2 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·AORTIC VALVULOPLASTY BALLOON DILATATION CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·AORTIC VALVULOPLASTY BALLOON DILATATION CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·AORTIC VALVULOPLASTY BALLOON DILATATION CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·BOSTON SCITNTIFIC SCIMED AORTIC VALVULOPLASTY(TM) CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER

    Syntec Femoral Nail System

    FDA UDI
    SYNTEC SCIENTIFIC CORPORATION·04712782906628·Syntec Internal Hex Captured Screw φ5.0 x L50mm

    Syntec Internal Hex Captured Screw

    FDA UDI
    SYNTEC SCIENTIFIC CORPORATION·04712782906895·Syntec Internal Hex Captured Screw φ5.0 x L50mm

    NIDEK UP-2000

    FDA 510(k)
    FDA Class 2 ·Radiology

    23GA COMBINED VITRECTOMY PACK WITH VALVES AND AFI AND WIDE FIELD ILLUMINATOR

    FDA Adverse Event
    Malfunction ·BAUSCH + LOMB·Product code HQC·May 31, 2019

    GOBED+

    FDA Adverse Event
    STRYKER MEDICAL QUEBEC LP·Product code FNL·October 19, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HLTHCARE CORP·Product code FRN·January 31, 2014

    ACS HI-TORQUE BALANCE MIDDLEWEIGHT GUIDE WIRE

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code DQX·December 19, 2012

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·LENS-WET(TM)

    Lens, Contact (Polymethylmethacrylate)

    FDA Pre-Market Approval
    FDA Unclassified ·BOSTON LENS(R) LENS - CLEAR

    Lens, Contact (Polymethylmethacrylate)

    FDA Pre-Market Approval
    FDA Unclassified ·BOSTON LENS(R) LENS - CLEAR

    Lens, Contact (Polymethylmethacrylate)

    FDA Pre-Market Approval
    FDA Unclassified ·BOSTON LENS(R) LENS - CLEAR