BEUDAMED
    23 results · 28ms · Sources: EU EUDAMED, US FDA

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    DILATOR, VESSEL, FOR PERC. CATHETER.

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Helix

    FDA UDI
    Nuvasive, Inc.·00887517137920·Helix R Screw, 4x13mm Var Self-Drill

    ZAVATION ROD CONNECTOR

    FDA UDI
    Zavation LLC·00197157016227·ROD CONNECTOR, PARALLEL CLOSED 10mm OFFSET, Ø 5...

    ZAVATION ROD CONNECTOR

    FDA UDI
    Zavation LLC·00197157016241·ROD CONNECTOR, PARALLEL CLOSED 14mm OFFSET, Ø 5...

    ZAVATION ROD CONNECTOR

    FDA UDI
    Zavation LLC·00197157016265·ROD CONNECTOR, PARALLEL CLOSED 18mm OFFSET, Ø 5...

    ZAVATION ROD CONNECTOR

    FDA UDI
    Zavation LLC·00197157016258·ROD CONNECTOR, PARALLEL CLOSED 16mm OFFSET, Ø 5...

    ZAVATION ROD CONNECTOR

    FDA UDI
    Zavation LLC·00197157016234·ROD CONNECTOR, PARALLEL CLOSED 12mm OFFSET, Ø 5...

    COOK AND COOK SPECTRUM CENTRAL VENOUS CATHETERS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    IVC THREE BLASTOCYST MEDIUM, CAT # 2007

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

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 16, 1998

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 16, 1998

    FENESTRATED BIPOLAR FORCEPSINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·May 8, 2014

    M2A-MAGNUM 42-50 TAPER INSERT STD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·October 23, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 11, 2007

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·August 22, 2022

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·July 3, 2018

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·July 3, 2018

    TRIPLE LUMEN POLYURETHANE CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQY·June 25, 2018

    Catheter, intravascular, therapeutic, short-term less than 30 days

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·November 10, 2022