BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    UCLA CCM Abutment

    FDA 510(k)
    FDA Class 2 ·Dental

    Edge™ Diamond FP016-4M (3.5) Football Pointed

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172003346·Diamond dental bur, reusable

    HORIZON PERINATAL CARE SURVEILLANCE AND ARCHIVAL MODEL VERSON 4.0

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

    ENDURAVENT-5 VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TPRLOC COCR CMTD STM T1 12.5MM

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDI·March 23, 2026

    CMK MOD 12/14 SZ202 L130

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·November 24, 2025

    OPTISENSE

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·January 11, 2014

    GYNECARE TVT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·June 27, 2013

    CVC KIT: 3-LUMEN 5.5 FR X 13 CM

    FDA Adverse Event
    Injury ·ARROW INTL., INC.·Product code DQO·September 26, 2008

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·May 1, 2024

    REVITAN, DISTAL PART, CURVED, UNCEMENTED, 24/200

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWY·July 20, 2023

    CMK MOD 12/14 SZ202 L130

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 8, 2026