L-Glutamine

GUDID 10190302003902

LIFE TECHNOLOGIES CORPORATION

Cell culture medium IVD

• Primary Device ID: 10190302003902
• NIH Device Record Key: cb0efb05-b1ac-4f38-bef6-6e2009549be5
• Commercial Distribution Discontinuation: 2020-03-27
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: L-Glutamine
• Version Model Number: 25030149
• Company DUNS: 118793157
• Company Name: LIFE TECHNOLOGIES CORPORATION
• 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: 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	10190302003902 [Primary]

FDA Product Code

• KIT: MEDIA AND COMPONENTS, SYNTHETIC CELL AND TISSUE CULTURE

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: 2020-05-01
• Device Publish Date: 2016-08-01

On-Brand Devices [L-Glutamine]

• 30190302003913: 25030081
• 10190302003902: 25030149