BEUDAMED
    Product Code: FJR FDA class 1 21 CFR 876.5540

    Forceps, Disconnect

    Gastroenterology, Urology

    The Disconnect Forceps is a hand instrument used to disconnect or separate components of shunt or catheter assemblies in urological and dialysis procedures. It is classified as FDA Class 1 (lowest risk) and is subject to general controls only. The product code is FJR, regulated under 21 CFR 876.5540 in the Gastroenterology and Urology specialty.

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    510(k)s
    0
    FEI Numbers
    10
    Registration Numbers
    10
    Unique Applicants
    0
    Years Active
    —

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    Basic Information

    Product Code
    FJR
    Device Class
    FDA class 1
    Regulation Number
    876.5540
    Medical Specialty
    Gastroenterology, Urology
    Review Panel
    GU
    Submission Type
    4

    Device Characteristics

    ✗
    GMP Exempt
    ✗
    Implant
    ✗
    Life Sustain/Support
    ✗
    Third Party
    —
    Summary Malfunction Reporting

    FEI Numbers

    This FDA classification entry is associated with 10 FEI numbers. Click on an entry to view related FDA registrations.

    Registration Numbers

    This FDA classification entry is associated with 10 registration numbers. Click on an entry to view related FDA registrations.