Paramount Medical Solutions

GUDID 00618125160976

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TIDI PRODUCTS, LLC

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• Primary Device ID: 00618125160976
• NIH Device Record Key: a678268c-3014-4061-9411-cb12a2e688ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Paramount Medical Solutions
• Version Model Number: 31432
• 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: true
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00618125160976 [Primary]
GS1	01618125160975 [Previous]
GS1	10618125160973 [Package]; Package: Case [50 Units]; In Commercial Distribution

FDA Product Code

• MMZ: Table, Cystometric, Electric

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: 2022-10-04
• Device Publish Date: 2022-09-26

On-Brand Devices [Paramount Medical Solutions]

• 00618125160976: Paramount Medical Solutions Urology Drain Bags Vinyl Fits Hoop Style Urology Frames 50 per Case
• 01618125160975: Paramount Medical Solutions Urology Drain Bags Vinyl Fits Hoop Style Urology Frames 50 per Case