RPMI Medium 1640 w/o L-Glutamine

GUDID 10190302004329

LIFE TECHNOLOGIES LIMITED

Cell culture medium IVD

• Primary Device ID: 10190302004329
• NIH Device Record Key: 95d6715c-77fc-45e6-8b11-5cb460308cbb
• Commercial Distribution Discontinuation: 2022-04-12
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: RPMI Medium 1640 w/o L-Glutamine
• Version Model Number: 32404014
• Company DUNS: 229044524
• Company Name: LIFE TECHNOLOGIES LIMITED
• 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	10190302004329 [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: 2022-04-21
• Device Publish Date: 2016-08-01

On-Brand Devices [RPMI Medium 1640 w/o L-Glutamine]

• 10190302004237: 31870017
• 10190302004329: 32404014