BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    M-OR

    DI: 00814005024394 · Model: M-OR · Quality Aspirators, Inc.
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Let the assistant research this device

    The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Brand Name
    M-OR
    Primary DI
    00814005024394
    Version / Model
    M-OR
    Catalog Number
    133-10026
    Company Name
    Quality Aspirators, Inc.
    Labeler DUNS
    121431159
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2025-02-27
    Public Version
    1
    Public Version Date
    2025-03-07
    Public Version Status
    New
    Public Device Record Key
    5380c573-1927-4756-b25c-83acc68a97a2

    Device Description

    M-OR

    Device Characteristics

    Single Use
    No
    Prescription Use (Rx)
    No
    Over the Counter (OTC)
    No
    Kit
    No
    Combination Product
    No
    HCT/P
    No
    Contains NRL
    No
    Not Made with NRL
    Yes
    MRI Safety
    MR Unsafe
    Direct Marking Exempt
    No
    PM Exempt
    Yes
    Has Serial Number
    No
    Has Lot/Batch Number
    Yes
    Has Manufacturing Date
    Yes
    Has Expiration Date
    No
    Has Donation ID
    No

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    KYT LIGHT, EXAMINATION, MEDICAL, BATTERY POWERED

    GMDN Terms

    Code Name
    46807 Head-worn lamp

    Identifiers

    Type ID
    Primary 00814005024394