DMEM/F12 Baxter Special 9, 500L BESP845L

GUDID 05407010126617

Lonza Verviers

Ex vivo cell culture medium

• Primary Device ID: 05407010126617
• NIH Device Record Key: 0c67699c-cd65-4e3d-8f42-271ca38b9605
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DMEM/F12 Baxter Special 9, 500L
• Version Model Number: BESP845L
• Catalog Number: BESP845L
• 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	05407010126617 [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: 2025-04-25
• Device Publish Date: 2025-04-17

Devices Manufactured by Lonza Verviers

• 05407010126549 - PBS - 1L bottle: 2025-04-25
• 05407010126556 - Lonza Perfusion Medium Base Powder 1 50L: 2025-04-25
• 05407010126563 - Lonza Perfusion Medium Base Powder1 100L: 2025-04-25
• 05407010126570 - Lonza Perfusion Medium Base Powder2 100L: 2025-04-25
• 05407010126587 - Lonza Perfusion Medium Base Powder2 200L: 2025-04-25
• 05407010126594 - New DMEM SPR_V01 - 5L: 2025-04-25
• 05407010126600 - DMEM/F12 Baxter Special 9, 1000L: 2025-04-25
• 05407010126617 - DMEM/F12 Baxter Special 9, 500L: 2025-04-25
• 05407010126617 - DMEM/F12 Baxter Special 9, 500L: 2025-04-25