SideKick™ 2

GUDID 00191506013684

Siliconized 10cm x 10mm x 18ga (1.2mm)

BOSTON SCIENTIFIC NEUROMODULATION CORPORATION

Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system Radio-frequency ablation system

• Primary Device ID: 00191506013684
• NIH Device Record Key: 6669592b-a627-4c8f-a27a-c505f0a79f02
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SideKick™ 2
• Version Model Number: RFK-C101018S-ZK2
• Company DUNS: 824951958
• Company Name: BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

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• Device Size Text, specify: 0
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• Device Size Text, specify: 0
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• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00191506013097 [Primary]
GS1	00191506013684 [Package]; Contains: 00191506013097; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• GXI: Probe, radiofrequency lesion

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-05-06
• Device Publish Date: 2021-04-28

On-Brand Devices [SideKick™ 2]

• 00191506013714: Siliconized 15cm x 10mm x 20ga (0.9mm)
• 00191506013707: Siliconized 15cm x 10mm x 18ga (1.2mm)
• 00191506013691: Siliconized 10cm x 10mm x 20ga (0.9mm)
• 00191506013684: Siliconized 10cm x 10mm x 18ga (1.2mm)