DMEM/F-12

GUDID 30190302001780

LIFE TECHNOLOGIES CORPORATION

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

• Primary Device ID: 30190302001780
• NIH Device Record Key: bd510341-1edd-4a51-947c-fe073ae8df61
• Commercial Distribution Discontinuation: 2022-05-25
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: DMEM/F-12
• Version Model Number: 11320033
• 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	10190302001786 [Primary]
GS1	30190302001780 [Package]; Contains: 10190302001786; Package: Case [10 Units]; Discontinued: 2022-05-25; Not in Commercial Distribution

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: 2022-05-26
• 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