Vesta

GUDID 10850040767251

Vesta RF Cannula

Stratus Medical LLC

Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation system probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use Percutaneous radio-frequency ablation probe cannula, single-use

• Primary Device ID: 10850040767251
• NIH Device Record Key: 01e1bf6b-f29d-4071-ab0b-2422ea5aa54b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vesta
• Version Model Number: NLT-100-20-10-CS
• Company DUNS: 117402924
• Company Name: Stratus Medical LLC
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00850040767094 [Primary]
GS1	10850040767251 [Package]; Contains: 00850040767094; Package: [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K190259

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: 2022-09-20
• Device Publish Date: 2022-09-12

On-Brand Devices [Vesta]

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• 40850040767221: Vesta RF Cannula
• 40850040767214: Vesta RF Cannula
• 40850040767207: Vesta RF Cannula
• 40850040767191: Vesta RF Cannula
• 40850040767184: Vesta RF Cannula
• 40850040767177: Vesta RF Cannula
• 40850040767160: Vesta RF Cannula
• 50850040767150: Vesta RF Cannula
• 40850040767146: Vesta RF Cannula
• 40850040767139: Vesta RF Cannula
• 50850040767129: Vesta RF Cannula
• 40850040767115: Vesta RF Cannula
• 40850040767108: Vesta RF Cannula
• 10850040767251: Vesta RF Cannula
• 40850040767085: Vesta RF Cannula
• 40850040767078: Vesta RF Cannula
• 40850040767061: Vesta RF Cannula
• 40850040767054: Vesta RF Cannula
• 50850040767044: Vesta RF Cannula