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

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    ClotTriever Thrombectomy System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bernafon

    FDA UDI
    Bernafon AG·05711584087565·ZR1, KIT IIC 10 85 BL ZERENA 1

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776199982·Graves ViewMai Speculum insulated medium

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694015417·2.0mm x 36mm Cannulated Lag Screw

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694070423·Cannulated 2.0 x 36mm Lag Screw Sterile Qty 5

    CALIX PC SPINAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DOCTOR SURGERY DIODE LASERS FAMILY

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CASSETTE MEDI RESERVOIR 12X100ML

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code LHI·January 18, 2022

    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

    AMK TIB INS SIZE 12 10MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·October 6, 2008

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 20, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011

    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