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

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    TIGER SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    n/a

    FDA UDI
    HANS RUDOLPH, INC.·00874750007141·4830C PNT NONHTD 400LPM 1.375

    16PW - Los Alamos - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588130583·16PW - Los Alamos - Poly White

    MULTIFUNCTION KEITO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BPA-FREE PIT AND FISSURE SEALANT

    FDA 510(k)
    FDA Class 2 ·Dental

    REMSTAR AUTO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

    REMSTAR PRO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

    REMSTAR AUTO A-FLEX W/HUMID

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code BZD·August 10, 2021

    REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS, FR

    FDA Adverse Event
    Injury ·RESPIRONICS, INC·Product code BZD·August 5, 2021

    BIPAP A30-S SILVER

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·September 25, 2024

    BIPAP A30, SILVER

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNS·September 25, 2024

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·May 18, 2011

    IMPAX CV OUTBOUDN(RESULTS MANGEMENT 2.08)

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP·Product code LLZ·February 28, 2014

    900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 9, 2013

    REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS,GER

    FDA Adverse Event
    Injury ·RESPIRONICS INC·Product code BZD·August 30, 2021

    Davol Salute Laproscopic 38cm Sterile Implant Cartridge, Sterile- 10 Q-ring;5/Box, Item Number: 0113058

    FDA Recall
    Terminated ·Davol, Inc., Sub. C. R. Bard, Inc.·Product code GDW·July 16, 2007

    BD BACTEC PLUS AEROBIC/F CULTURE VIALS (PLASTIC) -

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·April 3, 2024

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

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·August 29, 2025

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

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·August 29, 2025

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

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·August 29, 2025