GUDID 00813250017793

G4 Test Lead for Reference Jack

BOSTON SCIENTIFIC NEUROMODULATION CORPORATION

Radio-frequency ablation system

• Primary Device ID: 00813250017793
• NIH Device Record Key: b55a4cb6-5d1d-40b6-96da-d26d61c0de3a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: G4-TEST-REF
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813250017793 [Primary]

FDA Product Code

• GXD: GENERATOR, LESION, RADIOFREQUENCY

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-10-08
• Device Publish Date: 2017-08-21

Devices Manufactured by BOSTON SCIENTIFIC NEUROMODULATION CORPORATION

• 00191506048464 - GX1™: 2025-10-07 Radiofrequency Generator 2.0A, 120V
• 00191506048518 - GX1™: 2025-10-07 Radiofrequency Generator 2.0A, 220V
• 00191506048563 - GX1™: 2025-10-07 Radiofrequency Generator 2.0A, 240V
• 00191506059309 - GX1™: 2025-10-07 Radiofrequency Generator
• 00191506059330 - GX1™: 2025-10-07 GX1 RF GENERATOR HW 120V
• 00191506059347 - GX1™: 2025-10-07 GX1 RF GENERATOR HW 220V
• 00191506059354 - GX1™: 2025-10-07 GX1 RF GENERATOR HW 240V
• 08714729951254 - Spectra WaveWriter™: 2025-09-30 Implantable Pulse Generator Kit