STD ProCHO5 w/Pluronic w/o L-Gln or HT, 20L BE12-766P20

GUDID 05407010124231

Lonza Verviers

Ex vivo cell culture medium

• Primary Device ID: 05407010124231
• NIH Device Record Key: c6d96c78-5248-4b99-b66b-f1dbae850232
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STD ProCHO5 w/Pluronic w/o L-Gln or HT, 20L
• Version Model Number: BE12-766P20
• Catalog Number: BE12-766P20
• 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	05407010124231 [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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