BEUDAMED
    32 results · 38ms · Sources: EU EUDAMED, US FDA

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    TESTOSTERONE TEST SYSTEM; CALIBRATOR; AND QUALITY CONTROL MATERIAL (ASSAYED AND UNASSAYED)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MIRABAY

    FDA UDI
    Mirabay Orthodontics Corp.·05061075023146·KLEOS 2 PSL METAL HIGH TORQUE 022 LL12-LR12 PK5...

    DURAVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948006674·DURAVENT XL, SIZE 9

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193109886·HA PEEK EVOS Straight, ,9mmx8mmx 22mm , BICONVE...

    PATIENT CIRCUITS

    FDA UDI
    Zoll Medical Corporation·00847946023140·MASK, CPAP, #4, CHILD

    Ventlab

    FDA UDI
    VENTLAB, LLC·30889483271067·PVC Anesthesia Mask #4, Adult - M, 100/CA

    PATIENT CIRCUITS

    FDA UDI
    Zoll Medical Corporation·10847946023147·MASK, CPAP, #4, CHILD

    Occluder, Patent Ductus, Arteriosus

    FDA Pre-Market Approval
    FDA Class 3 ·NIT-OCCLUD PDA

    BRACE EZE

    FDA 510(k)
    FDA Class 1 ·Dental

    ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Occluder, Patent Ductus, Arteriosus

    FDA Pre-Market Approval
    FDA Class 3 ·NIT-OCCLUD PDA

    Occluder, Patent Ductus, Arteriosus

    FDA Pre-Market Approval
    FDA Class 3 ·PMA NIT-OCCLUD PDA

    Occluder, Patent Ductus, Arteriosus

    FDA Pre-Market Approval
    FDA Class 3 ·NIT-OCCLUD PDA

    Occluder, Patent Ductus, Arteriosus

    FDA Pre-Market Approval
    FDA Class 3 ·NIT-OCCLUD SYSTEM

    PREMICRON GREEN 3/0 (2) 17X45CM

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAT·April 7, 2022

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 16, 2025

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·May 20, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·May 26, 2011

    MICROSTAAR INJECTOR CARTRIDGE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL COMPANY·Product code KYB·August 14, 2008

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DQX·July 26, 2024