BEUDAMED
    117 results · 27ms · Sources: EU EUDAMED, US FDA

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    VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15); VNUS RFS FLEX, MODEL RFX-6-XX (XX = 10, 20, 30 & 40)

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

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00520031·

    Face-Cradle

    FDA UDI
    MERCURY ENTERPRISES, INC.·10641043520031·

    Aveta Waste Management Accessory

    FDA UDI
    MEDITRINA, INC.·00850006759446·Aveta Waste Management Accessory for use with A...

    PN Wearable Accessory L/XL Horizontal

    FDA UDI
    Curonix LLC·00850051034185·PNS Wearable Accessory L/XL Horizontal

    PNS Wearable Accessory L/XL Horizontal

    FDA UDI
    STIMWAVE TECHNOLOGIES INCORPORATED·00818225021867·Externally worn transmitter for the Wearable An...

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809841664·FOR MEN 15-20 MM HG KNEE HIGH CLOSED TOE EXTRA ...

    HDI 5000 ULTRASOUND SYSTEM WITH EXTENDED FIELD OF VIEW IMAGING

    FDA 510(k)
    FDA Class 2 ·Radiology

    DRG REACTION CHAMBER/SAFETY TIP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    FOCUS NIGHT & DAY

    FDA Adverse Event
    Injury ·P.T. CIBA VISION BATAM·Product code LPM·June 5, 2003

    SYNCHROMED EL

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code LKK·July 8, 2003

    HEARTMATE STROKE VOLUME LIMITER

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·June 20, 2003

    HEARTMATE STROKE VOLUME LIMITER

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·June 20, 2003

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·June 17, 2003

    *

    FDA Adverse Event
    Injury ·*·Product code LPL·May 22, 2003

    PROXIMATE INTRALUMINAL CIRCULAR STAPLER - 21MM

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code GAG·June 4, 2003

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·June 17, 2003

    HAKIM VALVE WITH INLINE RESERVOIR

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC./MEDOS S.A.·Product code JXG·September 8, 2003

    HOMECHOICE INTEGRATED APD SET WITH CASSETTE 3-PRONG

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code FKX·July 29, 2003

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQE·May 22, 2003