KnockOut™ SR Xenofree CTS™

GUDID 10190302002530

LIFE TECHNOLOGIES CORPORATION

Ex vivo cell culture medium

• Primary Device ID: 10190302002530
• NIH Device Record Key: 4bcd04ee-a7da-4cd7-b41c-d13433d4d887
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KnockOut™ SR Xenofree CTS™
• Version Model Number: 12618012
• Company DUNS: 118793157
• Company Name: LIFE TECHNOLOGIES CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10190302002530 [Primary]
GS1	30190302002534 [Package]; Package: Each [20 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K100616

FDA Product Code

• NDS: MEDIA, CULTURE, EX VIVO, TISSUE AND CELL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-12
• Device Publish Date: 2016-08-01

On-Brand Devices [KnockOut™ SR Xenofree CTS™]

• 10190302002547: 12618013
• 10190302002530: 12618012