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

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    AQUAMAX (ETAFILCON A) DISPOSABLE SOFT CONTACT LENSES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707008903·CALIBRA 1ST MOLAR BANDS n.UR 28

    OptiMesh Multiplanar Expandable Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7403120028·Short Articulating Curette

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197027151·Deaver Operating Scissors Fig. 3 straig...

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962106211·ø2.8mm STEINMANN PIN, 12", SINGLE TROCAR (ROUND...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197027120·Deaver Operating Scissors Fig. 3 straig...

    NEOTRACT ANCHOR SYSTEM MODEL TAS400

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

    6F MACH1/34356-XXX; 5F MACH1/35845-XXX; 7F MACH1/34357-XXX; 8F MACH1/34358-XXX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RADICAL 7

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·December 18, 2014

    RADICAL 7

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·December 18, 2014

    Widex

    FDA UDI
    Widex A/S·05706069796711·Widex EVOKE E-CIC (Clay brown ) 220, Right, RC ...

    Widex

    FDA UDI
    Widex A/S·05706069886870·WIDEX MOMENT M-XP (Clay brown ) 220, Telecoil

    Widex

    FDA UDI
    Widex A/S·05706069798012·Widex D-CIC (Clay brown ) Dream 220, Right, RC ...

    Widex

    FDA UDI
    Widex A/S·05706069888744·WIDEX MOMENT M-CIC (Clay brown ) 220, Right

    Widex

    FDA UDI
    Widex A/S·05706069796940·Widex EVOKE E-XP (Clay brown ) 220, Telecoil, R...

    RADICAL-7 COLOR SCREEN HANDHELD

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·May 29, 2015

    RDS3 DOCKING STATION

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·September 17, 2014

    DEPUY ASR XL FEM IMP SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 20, 2013

    ACCU-CHEK ® PERFORMA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 25, 2014

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 8, 2011