KH-020 BF-3 1000L Bag BESP1782P1000

GUDID 05407010129540

Lonza Verviers

Ex vivo cell culture medium

• Primary Device ID: 05407010129540
• NIH Device Record Key: e0b80051-9984-480f-8294-9cbabf90ed1b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KH-020 BF-3 1000L Bag
• Version Model Number: BESP1782P1000
• Catalog Number: BESP1782P1000
• 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	05407010129540 [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

• 05407010129656 - CD CHO Medium AGT-200Lbag filled to 100L: 2025-11-21
• 05407010129403 - KH-020 BF-6 1L Bag - Sample: 2025-11-19
• 05407010129410 - KH-020 BF-8 1L Sample Bag: 2025-11-19
• 05407010129427 - KH-020 BF-8 1000L Bag: 2025-11-19
• 05407010129434 - KH-020 BF-8 500L Bag: 2025-11-19
• 05407010129441 - KH-020 BF-9 1000L Bag: 2025-11-19
• 05407010129458 - KH-020 BF-9 1L Sample Bag: 2025-11-19
• 05407010129465 - KH-020 BF-9 500L Bag: 2025-11-19