K-Pack II Needle


Product Overview

K
K-Pack II - KN-2719RB500P


Device Description

A non-dedicated, sharp bevel-edged, hollow tubular device intended to be inserted beneath the skin of a patient while connected to a noninvasive device (e.g., syringe, secondary medication set) to administer and/or withdraw (aspirate) fluids/drugs; it may also be used for fluid/drug preparation. Some types are designed with a shielding mechanism (e.g., safety cap) for protection from sharp injuries. It is not specifically designed for blood collection or artery puncture, and does not have wings for fixation/placement (i.e., not a blood collection, intra-arterial, or venous butterfly needle). This is a single-use device.


Environmental Conditions

  • Special Storage Condition, Specify
    • Keep away from sunlight. Keep dry.
  • Storage Environment Temperature - Degrees Celsius
    • 30.00
    • 2.00

  • Device Sizes

  • Needle Outer Diameter: 0.4 Millimeter
  • Needle Length: 20 Millimeter
  • Needle Length: 0.75 Inch
  • Needle Gauge: 27 Gauge
  • Regular wall
    • Needle Outer Diameter: 0.4 Millimeter
    • Needle Length: 20 Millimeter
    • Needle Length: 0.75 Inch
    • Needle Gauge: 27 Gauge
    • Regular wall


    Device Sterilization

    Device Sterile: True

    Sterilization Prior To Use: False

    Sterilization Methods: No Data Available


    Product Codes

    Code: FMI

    Device Name: Needle, Hypodermic, Single Lumen

    Device Class: 2

    Physical State: N/A

    Definition: N/A

    Submission Type ID: 1

    Review Panel: HO

    Review Code: N/A

    Technical Method: N

    Gmp Exempt Flag: N/A

    Life Sustain Support Flag: N

    Unclassified Reason: N/A

    Implant Flag: N

    Target Area: N/A

    Regulation Number: 880.5570

    Third Party Flag: Y

    Medical Specialty: HO


    Device Identifiers

    Device Id: 55413206216739

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 35413206216735

    Package Quantity: 10

    Package Discontinue Date: N/A

    Package Status: In Commercial Distribution

    Package Type: Carton


    Device Id: 35413206216735

    Device Type: Package

    DeviceId Issuing Agency: GS1

    Contains DI Number: 05413206216734

    Package Quantity: 500

    Package Discontinue Date: N/A

    Package Status: In Commercial Distribution

    Package Type: Shelfbox


    Device Id: 05413206216734

    Device Type: Primary

    DeviceId Issuing Agency: GS1

    Contains DI Number: N/A

    Package Quantity: N/A

    Package Discontinue Date: N/A

    Package Status: N/A

    Package Type: N/A


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