Gibco

GUDID 10190302002363

LIFE TECHNOLOGIES CORPORATION

Ex vivo cell culture medium

• Primary Device ID: 10190302002363
• NIH Device Record Key: a8eab56f-5106-4afd-ae0a-bce93bf671c1
• Commercial Distribution Discontinuation: 2016-10-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Gibco
• Version Model Number: 12430112
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10190302002363 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• deNovo: DEN000008

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: 3
• Public Version Date: 2019-11-18
• Device Publish Date: 2016-08-01

On-Brand Devices [Gibco]

• 10190302002370: 12430120
• 10190302002363: 12430112
• 10190302005241: A2596102
• 10190302005234: A2596101
• 10190302002592: 12748018
• 10190302002585: 12747010