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

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    Filters Regulation: Us FDA ×

    Ti-one 101 TS Dental Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    VITREA 4DCT

    FDA 510(k)
    FDA Class 2 ·Radiology

    DISCOVRED

    FDA 510(k)
    FDA Class 2 ·Dental

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 10, 2025

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 30, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 5, 2025

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 13, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 14, 2026

    GMK-SPHERE TIBIAL INSERT FIXED FLEX SIZE 4/12 MM R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 3, 2019

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 18, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·May 19, 2025

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 8, 2025

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 30, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 31, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 6, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 14, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·March 30, 2026

    PERFUSOR®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·April 1, 2026

    APEX KNEE

    FDA Adverse Event
    Injury ·OMNILIFE SCIENCES, INC·Product code JWH·October 10, 2014