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

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    Medline Epidural Catheter

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HHM

    FDA UDI
    Oticon A/S·05707131281081·H160V2, MINIBTE 312 WL 85 STG HHM

    Symmetry Surgical Ultra®

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482055595·Ultra Instruments Clamp; Bulldog Artery Clamp; ...

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100196·MCINTYRE SPECULUM OPEN WIRE

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100202·NEVYAS DRAPE SPECULUM OPEN WIRE

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776087920·Ultra Bulldog Artery Clamp

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776087937·Ultra Bulldog Artery Clamp

    BOSWORTH AIR POLISHER

    FDA 510(k)
    FDA Class 1 ·Dental

    SEER LIGHT EXTEND COMPACT DIGITAL HOLTER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962111116·BULLDOG ARTERY CLAMP, 1 1/8", CVD, TITANIUM

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·January 7, 2016

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·December 15, 2016

    VERIFLEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·June 6, 2013

    ARCHITECT HAVAB-M

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code LOL·July 6, 2011

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

    MREYE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·COOK INC·Product code KRD·May 11, 2018

    MREYE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·COOK INC·Product code KRD·May 11, 2018

    MREYE EMBOLIZATION COIL

    FDA Adverse Event
    Injury ·COOK INC·Product code KRD·May 11, 2018