RPMI Medium 1640

GUDID 10190302004190

LIFE TECHNOLOGIES CORPORATION

Cell culture medium IVD

• Primary Device ID: 10190302004190
• NIH Device Record Key: 78b543cf-87d6-4b69-af0a-e847f1efd83c
• Commercial Distribution Discontinuation: 2019-10-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: RPMI Medium 1640
• Version Model Number: 31800022
• Company DUNS: 118793157
• Company Name: LIFE TECHNOLOGIES CORPORATION
• Device Count: 10
• 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	10190302004190 [Primary]
GS1	80190302004199 [Unit of Use]

FDA Product Code

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

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-12-12
• Device Publish Date: 2016-08-01

On-Brand Devices [RPMI Medium 1640]

• 10190302004213: 31800105
• 10190302004190: 31800022
• 10190302003841: 23400062
• 10190302003834: 23400021
• 10190302004206: 31800089
• 10190302002011: 11875176
• 10190302002004: 11875168
• 30190302001995: 11875085
• 30190302001988: 11875101
• 30190302001971: 11875093
• 30190302003760: 22400071
• 30190302003753: 22400089
• 10190302003742: 22400097
• 10190302005036: 72400153
• 10190302005029: 72400146
• 30190302005016: 72400047
• 10190302004893: 61870150
• 10190302004886: 61870143
• 30190302004873: 61870036
• 30190302003593: 21870084
• 30190302003586: 21870076