KH-020 BF-8 1000L Bag BESP1783P1000

GUDID 05407010129427

Lonza Verviers

Ex vivo cell culture medium

• Primary Device ID: 05407010129427
• NIH Device Record Key: ef2557a8-0b42-4e02-a6f8-0cf93fe2f892
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KH-020 BF-8 1000L Bag
• Version Model Number: BESP1783P1000
• Catalog Number: BESP1783P1000
• 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	05407010129427 [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: 2025-11-19
• Device Publish Date: 2025-11-11

Devices Manufactured by Lonza Verviers

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• 05407010129717 - Buffer C EZ-001 Module L : 1L Bag SAMPLE: 2025-12-31
• 05407010129724 - Buffer D EZ-001 Module L : 1L Bag SAMPLE: 2025-12-31
• 05407010129731 - Buffer E1 EZ-001 Module L : 1L Bag: 2025-12-31
• 05407010129748 - Buffer E1 EZ-001 Module L: 1L Bag SAMPLE: 2025-12-31
• 05407010129755 - Buffer G EZ-001 Module L : 1L Bag SAMPLE: 2025-12-31
• 05407010129762 - Buffer H EZ-001 Module L : 1L Bag SAMPLE: 2025-12-31
• 05407010129779 - Buffer I EZ-001 Module L : 1L Bag: 2025-12-31