Total Vein Systems

GUDID 00618125167890

Total Vein Systems Probe Covers Polyurethane Sterile 6.5in x 48in x 1in 50 per Case

TIDI PRODUCTS, LLC

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• Primary Device ID: 00618125167890
• NIH Device Record Key: e0a1d081-37bc-4651-b894-b842d7960245
• Commercial Distribution Discontinuation: 2023-03-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Total Vein Systems
• Version Model Number: 32373
• Company DUNS: 063519193
• Company Name: TIDI PRODUCTS, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00618125167890 [Package]; Contains: 01618125167899; Package: [50 Units]; Discontinued: 2023-03-10; Not in Commercial Distribution
GS1	01618125167899 [Primary]

FDA Product Code

• KKX: Drape, surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-03-13
• Device Publish Date: 2016-10-12

On-Brand Devices [Total Vein Systems]

• 00618125140893: Total Vein Systems Ultrasound Probe Cover Natural Polyurethane 6in x 48in 100 per Case
• 00618125157457: Total Vein Systems Probe Covers Polyurethane Sterile 6in x 96in x 1in 50 per Case
• 00618125167890: Total Vein Systems Probe Covers Polyurethane Sterile 6.5in x 48in x 1in 50 per Case
• 00618125141067: Total Vein Systems Ultrasound Probe Covers Natural Polyurethane Sterile 6in x 48in 50 per Case