CTS™ AIM-V™ Medium

GUDID 30190302014254

LIFE TECHNOLOGIES CORPORATION

Cell culture medium IVD

• Primary Device ID: 30190302014254
• NIH Device Record Key: aa27db88-30bb-4e3c-b3ab-d6d2ffa0a182
• Commercial Distribution Discontinuation: 2020-08-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: CTS™ AIM-V™ Medium
• Version Model Number: A3830801
• 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	10190302014250 [Primary]
GS1	30190302014254 [Package]; Contains: 10190302014250; Package: Case [6 Units]; Discontinued: 2020-08-10; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K022086

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: 7
• Public Version Date: 2020-08-11
• Device Publish Date: 2018-04-13

On-Brand Devices [CTS™ AIM-V™ Medium]

• 10190302014267: A3830802
• 30190302014254: A3830801