BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    NA

    DI: 00884838022041 · Model: 989803166021 · Philips Medical Systems Hsg
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    NA
    Primary DI
    00884838022041
    Version / Model
    989803166021
    Catalog Number
    989803166021
    Company Name
    Philips Medical Systems Hsg
    Labeler DUNS
    790605856
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2014-09-24
    Public Version
    6
    Public Version Date
    2023-07-06
    Public Version Status
    Update
    Public Device Record Key
    a1e09db6-015c-4215-8e94-7f7b20f30865

    Device Description

    HeartStart Adult/Child Pre-Connect Defib Pad

    Device Characteristics

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

    Sterilization

    Is Sterile
    No
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    MKJ Automated External Defibrillators (Non-Wearable)

    GMDN Terms

    Code Name
    44771 External defibrillation electrode, adult, single-use

    Identifiers

    Type ID
    Primary 00884838022041