BEUDAMED
    FDA UDI In Commercial Distribution 🇺🇸 United States

    Standard 64 Sublative iD (200 Pulse), 10 Pack

    DI: 00817495023786 · Model: KT72931 · Candela Corporation
    View on AccessGUDID
    Product Codes
    1
    GMDN Terms
    1
    Identifiers
    1
    Pkg Device Count
    1

    Basic Information

    Brand Name
    Standard 64 Sublative iD (200 Pulse), 10 Pack
    Primary DI
    00817495023786
    Version / Model
    KT72931
    Company Name
    Candela Corporation
    Labeler DUNS
    053468385
    Distribution Status
    In Commercial Distribution
    Device Count in Pkg
    1
    Record Status
    Published
    Publish Date
    2022-09-20
    Public Version
    4
    Public Version Date
    2023-07-20
    Public Version Status
    Update
    Public Device Record Key
    08338f0f-5d85-4257-9510-be59d576ace9

    Device Characteristics

    Single Use
    Yes
    Prescription Use (Rx)
    Yes
    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
    Yes
    Has Donation ID
    No

    Sterilization

    Is Sterile
    Yes
    Sterilization Prior Use
    No

    Product Codes

    Code Name
    GEI Electrosurgical, Cutting & Coagulation & Accessories

    GMDN Terms

    Code Name
    45220 Multi-modality skin surface treatment system

    Identifiers

    Type ID
    Primary 00817495023786