Lonza LVV Elution Buffer 08-993F

GUDID 00840075404392

Lonza Walkersville, Inc.

Cell culture buffered saline solution

• Primary Device ID: 00840075404392
• NIH Device Record Key: 9d32a9ee-5600-41f1-861f-54e1f7428174
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lonza LVV Elution Buffer
• Version Model Number: 08-993F
• Catalog Number: 08-993F
• Company DUNS: 609095955
• Company Name: Lonza Walkersville, Inc.
• 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: true
• 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	00840075404392 [Primary]

FDA Product Code

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

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-10-10
• Device Publish Date: 2024-10-02

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