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

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    AltiVate Anatomic to Reverse Conversion Module

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SUPER CHAIR FOR KIDS BY ORION

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    ANKYLOS TEMPORARY ABUTMENT BALANCE

    FDA 510(k)
    FDA Class 2 ·Dental

    BD NANO¿ 2ND GEN PEN NEEDLES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·February 14, 2022

    ACUSNARE POLYPECTOMY SNARE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code FDI·March 29, 2024

    ACUSNARE POLYPECTOMY SNARE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code FDI·March 29, 2024

    PRIME CARE (R) TRANSCEND BASIC MATTRESS

    FDA Adverse Event
    Malfunction ·PRIMUS MEDICAL LLC·Product code IKY·October 10, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 17, 2013

    WALLFLEX BILIARY RX PARTIALLY-COVERED STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·July 23, 2011

    BD BACTEC¿ PEDS PLUS¿/ F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Injury ·BECTON DICKINSON CARIBE LTD.·Product code MDB·April 2, 2026

    BD BACTEC¿ PEDS PLUS¿/ F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·February 16, 2026

    BD BACTEC¿ PEDS PLUS¿/ F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·October 9, 2024

    BD BACTEC¿ PEDS PLUS¿/ F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·October 10, 2024

    ACUSNARE POLYPECTOMY SNARE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code FDI·June 25, 2024

    Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 781271. 2. Model Number (REF): 782105. 510(k) Numbers: K173079, K183063, K193215, K213583, K223458, K251397, K251808.

    FDA Recall
    Open, Classified ·Philips North America·Product code LNH·April 14, 2026

    ACUSNARE POLYPECTOMY SNARE SOFT

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code FDI·September 3, 2024

    ACUSNARE POLYPECTOMY SNARE SOFT

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code FDI·September 3, 2024

    ACUSNARE POLYPECTOMY SNARE

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code FDI·July 26, 2024

    ACUSNARE POLYPECTOMY SNARE SOFT

    FDA Adverse Event
    Malfunction ·WILSON-COOK MEDICAL INC·Product code FDI·April 8, 2024

    BD BACTEC¿ PEDS PLUS¿/ F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·November 12, 2025