C3 CM3845

GUDID 05055273201611

A Complement C3 test system is a device intended for the quantitative in vitro determination of Complement C3 concentration in serum

RANDOX LABORATORIES LIMITED

Complement component C3 proactivator IVD, reagent

• Primary Device ID: 05055273201611
• NIH Device Record Key: 6bf3d0b2-abda-41f4-8d53-90749f910ed7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: C3
• Version Model Number: CM3845
• Catalog Number: CM3845
• Company DUNS: 227530649
• Company Name: RANDOX LABORATORIES LIMITED
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• 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

Customer Support Contacts

• Phone: +442894451070
• Email: technical.services@randox.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055273201611 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K000469

FDA Product Code

• CZW: Complement C3, Antigen, Antiserum, Control

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: 2019-12-23
• Device Publish Date: 2016-09-16

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