Evoke® RECAP Viewer 3045

GUDID 09352307000872

SALUDA MEDICAL PTY LIMITED

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• Primary Device ID: 09352307000872
• NIH Device Record Key: 09dafc23-9ccb-4f70-898b-013f3af10326
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Evoke® RECAP Viewer
• Version Model Number: 3045
• Catalog Number: 3045
• Company DUNS: 744596461
• Company Name: SALUDA MEDICAL PTY LIMITED
• 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: false
• Serial Number: false
• Manufacturing Date: false
• 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	09352307000872 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P190002

FDA Product Code

• LGW: Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-01-12
• Device Publish Date: 2023-01-04

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• 09352307001633 - Evoke® CAP12 Percutaneous Lead Kit - 90 cm: 2023-10-18
• 09352307001640 - Evoke® CAP12 Percutaneous Lead Kit - 60 cm: 2023-10-18
• 09352307001657 - Evoke® CAP12 Percutaneous Lead Kit - 90 cm: 2023-10-18
• 09352307001671 - Evoke® CAP12X Lead Extension Kit - 55 cm: 2023-10-18