Sodium Bicarbonate 7.5% - 500ml sample BESP1024P0.5

GUDID 05407010124309

Lonza Verviers

Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD Culture medium nutrient supplement IVD 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: 05407010124309
• NIH Device Record Key: 946cbdee-f8bc-4671-9ad5-19a4d6a3930e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sodium Bicarbonate 7.5% - 500ml sample
• Version Model Number: BESP1024P0.5
• Catalog Number: BESP1024P0.5
• 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	05407010124309 [Primary]

FDA Product Code

• JSK: Supplement, Culture Media

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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