BEUDAMED
    19 results · 31ms · Sources: EU EUDAMED, US FDA

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    Vein Clamps, Artery Clamps

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DD tempMED

    FDA UDI
    Dental Direkt GmbH·EDDIK113151·DD tempMED are pre-colored dental milling blank...

    McKesson

    FDA UDI
    MCKESSON MEDICAL-SURGICAL INC.·00612479255944·PUNCH BIOPSY DISP 6MM

    STRYKER CMF MEDPOR CUSTOMIZED IMPLANT

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

    MULTIPURPOSE DRAINAGE CATHETER

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

    DEPUY (JOHNSON & JOHNSON)

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS·Product code JWH·August 4, 2003

    EXPECT PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·May 19, 2026

    EXPECT PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·September 24, 2025

    ACQUIRE? PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·October 10, 2025

    EXPECT PULMONARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·November 14, 2024

    EXPECT PULMONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FCG·April 14, 2026

    ZYNO PUMPS

    FDA Adverse Event
    Injury ·ZYNO MEDICAL, LLC·Product code FRN·May 21, 2024

    5.0MM TRANSPEDICULAR SCHANZ SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code NKB·June 11, 2013

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011

    CAROTID WALLSTENT MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code NIM·September 11, 2008

    SARS-COV-2 IGM

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND·Product code QKO·October 26, 2020

    ZYNO MEDICAL Z-800 INFUSION PUMP SYSTEM

    FDA Adverse Event
    Injury ·ZYNO MEDICAL, LLC·Product code FRN·January 21, 2025

    ZYNO MEDICAL Z-800 INFUSION PUMP SYSTEM

    FDA Adverse Event
    Injury ·ZYNO MEDICAL, LLC·Product code FRN·July 9, 2024

    Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH, Professor-Kuntscher-Str. 1-5, 24232 Schonkirchen Germany. Distributed in the USA by Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The T2 Arthrodesis Nail is intended for the treatment of Knee Arthrodesis. The design of the T2 Arthrodesis Nail features a unique curvature which incorporates both femur ante curvature and knee valgus bend. Indications: Aseptic failed total knee arthro-plasty with or without bone loss; Failed external fixation, non unions and malunions; Periarticular fractures where repair is not possible; Pathologic fractures and tumor resections; Pseudoarthrosis and correct osteotomy; Ipsilateral femur fractures; and Open and closed femoral fractures.

    FDA Enforcement
    Class II ·Terminated·Stryker Howmedica Osteonics Corp.·July 25, 2012