GIBCO® CTS™ AIM V® SFM

GUDID 10190302005081

LIFE TECHNOLOGIES CORPORATION

Cell culture medium IVD

• Primary Device ID: 10190302005081
• NIH Device Record Key: 4ea2f2e8-fbb8-4561-8c5b-f0f825248ba6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GIBCO® CTS™ AIM V® SFM
• Version Model Number: 0870112BK
• 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	10190302005081 [Primary]

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: 4
• Public Version Date: 2019-11-18
• Device Publish Date: 2016-08-01

On-Brand Devices [GIBCO® CTS™ AIM V® SFM]

• 10190302005098: 0870112DK
• 10190302005081: 0870112BK