Bulk Packaged sterile filtered WFI-20L BE02-038P20

GUDID 05407010122510

Lonza Verviers

Ex vivo cell culture medium

• Primary Device ID: 05407010122510
• NIH Device Record Key: 70ef652b-48b3-49c7-8e62-79ba131e8b1f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bulk Packaged sterile filtered WFI-20L
• Version Model Number: BE02-038P20
• Catalog Number: BE02-038P20
• 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	05407010122510 [Primary]

FDA Product Code

• PPM: General Purpose Reagent

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-05-27
• Device Publish Date: 2022-12-09

On-Brand Devices [Bulk Packaged sterile filtered WFI-20L]

• 05407010124606: BE02-038P20C
• 05407010122510: BE02-038P20