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

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    STERILE NITRILE POWDER FREE EXAMINATION GLOVE(VBLU), STERLE NITRILE POWDER FREE EXAMINATION GLOVE(ABLU)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NexxZr™ T / D-100-20-NT-A100-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271112163·

    MEGA PLUS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809665580061·Rod(CoCr), Ø6.0 x 60mm

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197303866·Zoellner Ear Specual outer ...

    RAVINE Lateral Access System

    FDA UDI
    VB Spine LLC·10888857560529·Lateral Access Blade Size 24x120 mm

    HAMILTON-TC1

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CRYOMEGA

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

    SELOX ST 53

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH AND CO·Product code DTB·July 21, 2006

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB C.R. BARD, INC.·Product code GDW·March 29, 2006

    TRILOGY ACETABULAR SYSTEM SHELL WITH CLUSTER HOLES POROUS

    FDA Adverse Event
    Injury ·ZIMMER MFG. B.V.·Product code JDI·April 22, 2006

    SYNCHROMED EL

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code LKK·January 20, 2006

    JOSTENT GRAFTMASTER

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH·Product code MAF·March 16, 2006

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code NIM·June 8, 2006

    VNUS VAREX PHLEBECTOMY INSTRUMENT

    FDA Adverse Event
    Malfunction ·VNUS MEDICAL TECHNOLOGIES, INC.·Product code DQO·April 3, 2006

    COAGUCHEK PT TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·March 10, 2006

    HIRES 90K

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS CORP.·Product code MCM·March 15, 2006

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC, INC, NEUROLOGICAL DIVISION·Product code LKK·April 11, 2006

    CLAVE SYSTEM W/ REMOVABLE CAP

    FDA Adverse Event
    Other ·HOSPIRA WORLDWIDE INC·Product code FPA·June 15, 2006

    POLYROX 53/15 BP

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code DTB·July 17, 2006

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·April 12, 2006