CO2 Alkaline Buffer

GUDID 00811403011674

Diamond Diagnostics Inc.

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• Primary Device ID: 00811403011674
• NIH Device Record Key: eb163c21-c9a6-4c38-9d37-3bd4d1bdffb8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CO2 Alkaline Buffer
• Version Model Number: BK-472515D
• 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: 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	00811403011674 [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 [CO2 Alkaline Buffer]

• 00811403011087: For the quantitative determination of total CO2 in serum and plasma.
• 00811403011674: BK-472515D