ProDoma 3 (KF10) w/o L-Glutamine 20L ba BESP1370P20

GUDID 05407010128789

Lonza Verviers

Ex vivo cell culture medium

• Primary Device ID: 05407010128789
• NIH Device Record Key: f069264b-3fc8-412f-bea5-0621064da5f8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProDoma 3 (KF10) w/o L-Glutamine 20L ba
• Version Model Number: BESP1370P20
• Catalog Number: BESP1370P20
• 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	05407010128789 [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: 2025-09-23
• Device Publish Date: 2025-09-15

Devices Manufactured by Lonza Verviers

• 05407010128994 - DMEM Glutamax 2% SRPT - 500ml bag SAMPLE: 2025-10-07
• 05407010129007 - 0.2M NaCl - 500 ml bag: 2025-10-07
• 05407010129014 - Buffer DEN-C - 1000L bag: 2025-10-07
• 05407010129021 - Buffer DEN-C - 1L bag SAMPLE: 2025-10-07
• 05407010128796 - Wet Process Wash Buffer, 50L bag: 2025-10-06
• 05407010128802 - Bulk Packaged sterile filtered WFI - 10L: 2025-10-06
• 05407010128819 - Bulk Packaged sterile filtered WFI -100L: 2025-10-06
• 05407010128826 - Bulk Packaged sterile filtered WFI-1LSAM: 2025-10-06