BEUDAMED
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    HANCOCK AORTIC PUNCH

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    Helix

    FDA UDI
    Nuvasive, Inc.·00887517134905·Helix R Plate, 22mm 1-Level

    BaseVac

    FDA UDI
    R. E. Morrison Equipment Inc·D13028001220·2HD4.40A | 8 User Dual Pump System | 2 Hp (x2) ...

    THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope

    FDA UDI
    THD SPA·08033737710593·The THD Light-Scope rectoscope is a disposable ...

    Convaid

    FDA UDI
    CONVAID PRODUCTS, INC.·10840117400815·

    Convaid

    FDA UDI
    CONVAID PRODUCTS, INC.·00840117408449·

    ORTHO ARCH

    FDA UDI
    Ortho Arch Company Inc·D90980012210·MATHIEU NEEDLE HOLDER W/ SAFETY LATCH - REGULAR...

    Opaque

    FDA UDI
    Kerr Corporation·00841396107986·Resin Based Dental Restorative Material - C4

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209100477·KIT, HIGH RISK WARRANT CASUALTY - ODG

    ACUMED

    FDA UDI
    Acumed LLC·10806378040054·Universal Tray Screw Caddy

    ADP,1,P800,S800,1/4" BE,N,RLD & DUKANE

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828132756·ADP,1,P800,S800,1/4" BE,N,RLD & DUKANE

    SOPRO 670 ARTHROSCOPIC PUMP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COLLAGRAFT STRIP BONE GRAFT MATRIX (FOR USE AS A BONE FILLER), MODEL 1X,3X,6X (1,3 OR 6 STRIPS PER BOX)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    I-STAT ACT KAOLIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE INC.·Product code JBP·March 18, 2026

    11MM/130 DEG TI CANN TFNA 420MM/LEFT - STERILE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HSB·June 27, 2025

    CORAIL2 STD SIZE 10

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code KWA·May 8, 2014

    LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·October 22, 2012

    PANALOK LOOP ANCHOR

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code MBI·August 10, 2010

    MOTO PARTIAL KNEE ANATOMICAL FEMORAL COMPONENT CEMENTED S5 RM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·March 8, 2024

    Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021