Shanghai Beijin

GUDID 06975756090022

EDEN FED MEDIUM B

Shanghai Beijin Biotechnological Co., LTD

Cell culture medium IVD

• Primary Device ID: 06975756090022
• NIH Device Record Key: 7bf31c1a-8aca-4a84-a507-9863b513c917
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Shanghai Beijin
• Version Model Number: EDEN FED MEDIUM B
• Company DUNS: 416877204
• Company Name: Shanghai Beijin Biotechnological Co., LTD
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06975756090022 [Primary]

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-11-15
• Device Publish Date: 2022-11-07

On-Brand Devices [Shanghai Beijin]

• 06975756090022: EDEN FED MEDIUM B
• 06975756090015: EDEN FED MEDIUM A
• 06975756090008: EDEN BASAL MEDIUM