BEUDAMED
    16 results · 21ms · Sources: EU EUDAMED, US FDA

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    HUMERAL HEAD, MANUAL DRIVER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694008372·2.4mm x 22mm Lag Screw

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694000833·2.4mm x 22mm Screw

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111077517·PEDIATRIC DUAL STETH 30" BLUE

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694035149·2.4 x 22mm Lag Screw, Sterile

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694062893·2.4 x 22mm Screw Sterile Qty 2

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694067003·HPS 2.4 x 22mm Lag Screw Sterile Qty 5

    VARPR 3.5MM 90 SUCTION ELECTRODE FOR USE WITH VAPR SYSTEM

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

    K-ASSAY D-DIMER CONTROLS

    FDA 510(k)
    FDA Class 2 ·Hematology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 21, 2026

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 14, 2025

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 16, 2013

    EXTRACTOR ASNIS III FOR SCREWS:Ø4.0MM AO FITTING

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code LXH·September 5, 2014

    M-1 COT - BASE HIGH LOAD 28

    FDA Adverse Event
    Injury ·STRYKER MEDICAL·Product code FPO·April 6, 2011

    Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

    FDA Enforcement
    Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012

    CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measured drug therapy to patients in hospital or outpatient settings.

    FDA Enforcement
    Class II ·Terminated·Smiths Medical ASD, Inc.·June 24, 2015