Wet Process Wash Buffer, 50L bag BESP1356P50

GUDID 05407010128796

Lonza Verviers

Ex vivo cell culture medium

• Primary Device ID: 05407010128796
• NIH Device Record Key: 57b72657-ab88-4643-95a3-194f3d487127
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Wet Process Wash Buffer, 50L bag
• Version Model Number: BESP1356P50
• Catalog Number: BESP1356P50
• 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	05407010128796 [Primary]

FDA Product Code

• PPM: General Purpose Reagent

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-10-06
• Device Publish Date: 2025-09-26

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
• 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