MEM Earles

GUDID 10190302004831

LIFE TECHNOLOGIES CORPORATION

Cell culture medium IVD

• Primary Device ID: 10190302004831
• NIH Device Record Key: cc49cb29-e1a4-4b4c-9326-0b8398ade04b
• Commercial Distribution Discontinuation: 2019-10-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MEM Earles
• Version Model Number: 61100061
• 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	10190302004831 [Primary]
GS1	80190302004830 [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 [MEM Earles]

• 10190302004831: 61100061
• 10190302004701: 51200038
• 10190302002318: 12360038
• 30190302001667: 11095072
• 30190302001650: 11095080
• 30190302001643: 11090081
• 10190302001632: 11090073