DMEM/F-12

GUDID 10190302001816

LIFE TECHNOLOGIES CORPORATION

Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD Cell culture medium IVD

• Primary Device ID: 10190302001816
• NIH Device Record Key: 8804ac55-7659-494b-aefe-d3eb42130566
• Commercial Distribution Discontinuation: 2022-04-29
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: DMEM/F-12
• Version Model Number: 11330107
• 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	10190302001816 [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: 2022-05-09
• Device Publish Date: 2016-08-01

On-Brand Devices [DMEM/F-12]

• 10190302002417: 12500096
• 10190302002400: 12500062
• 10190302002332: 12400024
• 10190302001816: 11330107
• 10190302001809: 11330099
• 30190302001797: 11330032
• 30190302001780: 11320033