HDL Ultra Cholesterol Reagent SK6122-20

GUDID 00628063400614

SEKISUI DIAGNOSTICS, LLC

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• Primary Device ID: 00628063400614
• NIH Device Record Key: 4764623b-74ca-466e-bc58-0308d99583e8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HDL Ultra Cholesterol Reagent
• Version Model Number: SK6122-20
• Catalog Number: SK6122-20
• 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	00628063400614 [Primary]

FDA Product Code

• LBS: LDL & VLDL PRECIPITATION, CHOLESTEROL VIA ESTERASE-OXIDASE, 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

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