Bulk Packaged sterile filtered WFI-20L BE02-038P20C

GUDID 05407010124606

Lonza Verviers

Ex vivo cell culture medium

• Primary Device ID: 05407010124606
• NIH Device Record Key: 6464e13b-cc7b-439c-9cad-464e936b9c30
• Commercial Distribution Discontinuation: 2023-03-03
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Bulk Packaged sterile filtered WFI-20L
• Version Model Number: BE02-038P20C
• Catalog Number: BE02-038P20C
• 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	05407010124606 [Primary]

FDA Product Code

• KIT: Media And Components, Synthetic Cell And Tissue Culture
• 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: 3
• Public Version Date: 2023-03-06
• Device Publish Date: 2022-12-09

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

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