Reference Electrode

GUDID 00811403018772

Diamond Diagnostics Inc.

Reference electrode IVD

• Primary Device ID: 00811403018772
• NIH Device Record Key: 197c09bd-e189-4f83-80d8-95c28d242fa1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reference Electrode
• Version Model Number: AW-906179D
• 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: true
• 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	00811403018772 [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: 2023-06-19
• Device Publish Date: 2023-06-10

On-Brand Devices [Reference Electrode]

• 00811403010448: To aide in measurements of Na+, K+, Cl-, Ca++, and Li+ in whole blood, plasma, serum and diluted
• 00811403015801: ME-2103D
• 00811403018772: AW-906179D
• 00811403017720: RD-945633D
• 00811403017713: RD-945389D
• 00811403011865: BM-373039D
• 00811403017089: OY-MU9197D
• 00811403013326: CD-476273D