N-geneous LDL Cholesterol Reagent (R1) 80-4604-00

GUDID 00628063400690

SEKISUI DIAGNOSTICS, LLC

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• Primary Device ID: 00628063400690
• NIH Device Record Key: 7122f111-c05a-4556-858e-59c763cf971b
• Commercial Distribution Discontinuation: 2016-10-24
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: N-geneous LDL Cholesterol Reagent (R1)
• Version Model Number: 80-4604-00
• Catalog Number: 80-4604-00
• Company DUNS: 966812344
• Company Name: SEKISUI DIAGNOSTICS, LLC
• 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: 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	00628063400690 [Primary]

FDA Product Code

• LBR: LDL & VLDL PRECIPITATION, HDL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-20

On-Brand Devices [N-geneous LDL Cholesterol Reagent (R1)]

• 00628063400690: 80-4604-00
• 00628063400676: 80-4598-00