Copan Universal Transport Medium (UTM-RT) System 3C075N

GUDID 08053326010446

Copan Universal Transport Medium (UTM-RT) System 3 ml

COPAN ITALIA SPA

General specimen container IVD, additive/medium

• Primary Device ID: 08053326010446
• NIH Device Record Key: 904782b8-a9e3-45f1-9c5b-00369f2ad1ff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Copan Universal Transport Medium (UTM-RT) System
• Version Model Number: 3C075N
• Catalog Number: 3C075N
• Company DUNS: 428981112
• Company Name: COPAN ITALIA SPA
• Device Count: 50
• 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	08053326010446 [Unit of Use]
GS1	38053326010447 [Primary]

FDA Product Code

• JSM: Culture Media, Non-Propagating Transport

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: 2025-06-05
• Device Publish Date: 2025-05-28

On-Brand Devices [Copan Universal Transport Medium (UTM-RT) System]

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• 18053326010283: Copan Universal Transport Medium (UTM-RT) System 3ml + One regular flocked swab, breaking point
• 18053326009867: Copan Universal Transport Medium (UTM-RT) System 3ml + One flexible flocked swab, breaking point
• 58053326009551: Copan Universal Transport Medium (UTM-RT) System 3ml