BD Universal Viral Transport 220244

GUDID 58053326009377

1 mL Vial

COPAN ITALIA SPA

General specimen container IVD, additive/medium General specimen container IVD, additive/medium General specimen container IVD, additive/medium General specimen container IVD, additive/medium

• Primary Device ID: 58053326009377
• NIH Device Record Key: f1085584-5191-4ee4-8c5a-3afbff31e81e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BD Universal Viral Transport
• Version Model Number: 220244
• Catalog Number: 220244
• 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	08053326009372 [Unit of Use]
GS1	38053326009373 [Primary]
GS1	58053326009377 [Package]; Contains: 38053326009373; Package: [6 Units]; In Commercial Distribution

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: 2022-12-15
• Device Publish Date: 2022-12-07

On-Brand Devices [BD Universal Viral Transport]

• 58053326009421: 3 mL Vial, Flock Flex Mini
• 58053326009414: 3 mL Vial, Flock Mini
• 58053326009384: 1 mL Vial, Flock Flex Mini
• 58053326009377: 1 mL Vial
• 58053326009346: 3 mL Vial, Standard Kit