BEUDAMED
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    MONARCH II IOL DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    Biim iOS App, P1.2

    FDA UDI
    Biim Ultrasound AS·07090045490143·Biim iOS App, P1.2

    Creation Willi Geller

    FDA UDI
    KLEMA Dentalprodukte GmbH·ECWG0011571·In Nova Neo INN-7 grey

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496001157·MAGIC 50, SIZE S, FUMO, TIGHTS WITH A THREE-DIM...

    Creation Willi Geller

    FDA UDI
    KLEMA Dentalprodukte GmbH·09010782022047·In Nova Neo INN-7 grey

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001157·artVeneer life lower anteriors, UBM, A4

    UniPlex® NanoLine®

    FDA UDI
    Pajunk GmbH Medizintechnologie·04048223070055·UniPlex® NanoLine® UP 3/080, 22G (0,70) x 80mm ...

    UniPlex® NanoLine®

    FDA UDI
    Pajunk GmbH Medizintechnologie·04048223070093·UniPlex® NanoLine® UP 3/100, 21G (0,80) x 100mm...

    UniPlex® NanoLine®

    FDA UDI
    Pajunk GmbH Medizintechnologie·04048223070062·UniPlex® NanoLine® UP 3/50, 22G (0,70) x 50mm, ...

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918118079·Radial Femoral Angiography Drape_4 fenestrated_...

    N/A

    FDA UDI
    Doppkon GmbH & Co. KG·04262494463099·Angled Bullet Handle 106mm x 50mm

    AGILENT INFORMATION CENTER SOFTWARE FOR M3150A AND M3153A AND AGILENT M2/M3/M4 COMPACT PORTABLE PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FRESENIUS COMBILINES LOW VOLUME BLOOD TUBING SET, MODELS 03-2291 (POST PUMP) AND 03-2292 (PRE-PUMP)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 25, 2025

    9616240-2006-00341

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    LDWR,ECG ESIS PINCH,DOM,5L,50"

    FDA UDI
    Datascope Corp.·10607567104706·LDWR,ECG ESIS PINCH,DOM,5L,50"

    LDWR,ECG ESIS PINCH,INT,5L,50"

    FDA UDI
    Datascope Corp.·10607567105529·LDWR,ECG ESIS PINCH,INT,5L,50"

    9616240-2006-00332

    FDA Adverse Event
    Other ·Product code FII·June 1, 2006

    INFILTRALONG CATHETER

    FDA Adverse Event
    Malfunction ·PAJUNK GMBH MEDIZINTECHNOLOGIE·Product code BSO·May 24, 2019

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 25, 2025