BUN Reagent

GUDID 00811403011650

Diamond Diagnostics Inc.

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• Primary Device ID: 00811403011650
• NIH Device Record Key: e0da2d2f-e6ff-4696-9242-6b8f30f4d046
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BUN Reagent
• Version Model Number: BK-472482D
• Company DUNS: 947514303
• Company Name: Diamond Diagnostics Inc.
• 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: true
• Device Combination Product: false
• Single Use: false
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00811403011650 [Primary]

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: 2023-06-20
• Device Publish Date: 2023-06-12

On-Brand Devices [BUN Reagent]

• 00811403011124: For the quantitative determination of urea nitrogen in serum or plasma.
• 00811403011650: BK-472482D