BEUDAMED
    17 results · 29ms · Sources: EU EUDAMED, US FDA

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    NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE

    FDA 510(k)
    FDA Class 1 ·Radiology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123274·K-WIRE - DOUBLE TROCAR 1.8mm DIA x 150mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123847·K-WIRE - DOUBLE TROCAR 1.8mm DIA x 200mm

    SAVINA 300 SAVINA 300, COUNTRY VARIANTS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OLYMPUS ULTRASONIC GASTROVIDEOSCOPE GF TYPE UC140P-DO5 & OLYMPUS ULTRASONIC GASTROFIBERSCOPE GF TYPE UC30P

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MCS + 8150

    FDA Adverse Event
    Malfunction ·HAEMONETICS CORP.·Product code GKT·January 15, 2013

    BASIC CONFIGURATION MODEL 6100 BASE

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIVISION·Product code FPO·December 7, 2010

    UNKNOWN

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·July 9, 2014

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·July 30, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·November 24, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·July 15, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 9, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 4, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 24, 2025

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·January 12, 2026

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·March 4, 2026

    PCCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·February 19, 2026