BEUDAMED
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    PERFECTA AND EXTEND

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Solus Laryngeal Mask Airway Kit, Size 4

    FDA UDI
    Intersurgical Incorporated·00816472021609·Solus Laryngeal Mask Airway Kit, Size 4

    artegral life HD

    FDA UDI
    Merz Dental GmbH·D7092004032·artegral life HighDefinition posterior upper -M...

    ImmunoDOT Leptospira IgM

    FDA UDI
    GenBio·00613745000169·The GenBio IgM ImmunoDOT Leptospira test is a q...

    NorthStar

    FDA UDI
    Seaspine Orthopedics Corporation·10889981196264·Poly. Screw, 4.0mm x 32mm

    Medical Facets NC

    FDA UDI
    MEDICAL FACETS NC LLC·M933MDF20040320·2.0mm Cortex Screw, 1.5 Hex, Self-Tapping, 32mm

    Biozip

    FDA UDI
    STRYKER CORPORATION·04546540392428·5.0MM BIOZIP DRILL 3.25MM X 13.5MM

    Cortium Universal OCT Spinal Fixation System

    FDA UDI
    Ulrich Medical Usa, Inc.·00814386026208·Smooth shank screw, Ø 4.0mm, length 32mm, high ...

    RESPONSE 2000 CEMENTED HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LEVEEN NEEDLE ELECTRODE

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

    MAMMARY IMPLANT

    FDA Adverse Event
    DOW CORNING CORP.·Product code FTR·November 15, 1994

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF004032290931317201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF004032290932517201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF004032290933517201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF004032290931117201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF004032290932117201·BTE-TRT

    audifon

    FDA UDI
    audifon GmbH & Co. KG·EADF004032290931517201·BTE-TRT

    COBAS® LIAT® SARS-COV-2 & INFLUENZA A/B

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QLT·October 15, 2021

    UNKNOWN DEPUY FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWY·March 14, 2013

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 7, 2011