ModProCHO5 w/8mM L-Gln,0.25% Pluro 500mL BESP1417P0.5

GUDID 05407010128499

Lonza Verviers

Ex vivo cell culture medium

• Primary Device ID: 05407010128499
• NIH Device Record Key: 502316be-1a83-4022-bc05-ad416dc3a9f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ModProCHO5 w/8mM L-Gln,0.25% Pluro 500mL
• Version Model Number: BESP1417P0.5
• Catalog Number: BESP1417P0.5
• Company DUNS: 370158847
• Company Name: Lonza Verviers
• 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: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05407010128499 [Primary]

FDA Product Code

• KIT: Media And Components, Synthetic Cell And Tissue Culture

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: 2025-08-28
• Device Publish Date: 2025-08-20

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