GLS SPE - 500ml sample bag BESP531P0.5

GUDID 05407010124378

Lonza Verviers

Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium Ex vivo cell culture medium

• Primary Device ID: 05407010124378
• NIH Device Record Key: 5af6e9f2-a3f6-4557-a8ce-348a6f22a91e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GLS SPE - 500ml sample bag
• Version Model Number: BESP531P0.5
• Catalog Number: BESP531P0.5
• 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	05407010124378 [Primary]

FDA Product Code

• KIT: Media And Components, Synthetic Cell And Tissue Culture

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: 2023-03-03
• Device Publish Date: 2022-12-09

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