Paramount Medical Solutions

GUDID 01618125160975

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TIDI PRODUCTS, LLC

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• Primary Device ID: 01618125160975
• NIH Device Record Key: ef471908-904a-4318-84ae-e6cd6dbf8f3e
• Commercial Distribution Discontinuation: 2022-09-22
• Commercial Distribution Status: Not 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: 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	01618125160975 [Primary]

FDA Product Code

• MMZ: TABLE, CYSTOMETRIC, ELECTRIC

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-02-05
• Device Publish Date: 2016-10-12

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