SF5-16 med. with Pluronic Biograde -Sup1 BESP1760SUP1L

GUDID 05407010125665

Lonza Verviers

Cell culture medium IVD

• Primary Device ID: 05407010125665
• NIH Device Record Key: 5309ef53-27a7-4958-ac03-6b5e8c091fc2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SF5-16 med. with Pluronic Biograde -Sup1
• Version Model Number: BESP1760SUP1L
• Catalog Number: BESP1760SUP1L
• 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	05407010125665 [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: 2025-01-14
• Device Publish Date: 2025-01-06

On-Brand Devices [SF5-16 med. with Pluronic Biograde -Sup1]

• 05407010125696: BESP1760SUP1B
• 05407010125665: BESP1760SUP1L