Sodium Electrode

GUDID 00811403015795

Diamond Diagnostics Inc.

Sodium (Na+) electrode IVD

• Primary Device ID: 00811403015795
• NIH Device Record Key: d36d7dc4-7ddf-4082-a828-7e5c85182a79
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sodium Electrode
• Version Model Number: ME-2102D
• 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: false
• Device Combination Product: false
• Single Use: true
• 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	00811403015795 [Primary]

FDA Product Code

• JGS: Electrode, Ion Specific, Sodium

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: 2023-06-13
• Device Publish Date: 2023-06-05

On-Brand Devices [Sodium Electrode]

• 00811403015795: ME-2102D
• 00811403010165: Measuring concentration of Sodium in whole blood, serum, plasma, and diluted urine samples.
• 00811403018789: AW-903393D
• 00811403012541: BM-371037D
• 00811403011490: BK-668295D
• 00811403017058: OY-MU9194D