Potassium Electrode

GUDID 00811403012558

Diamond Diagnostics Inc.

Potassium (K+) electrode IVD

• Primary Device ID: 00811403012558
• NIH Device Record Key: 7b644fa1-fb6c-4032-a026-09e5480004c4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Potassium Electrode
• Version Model Number: BM-371038D
• 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	00811403012558 [Primary]

FDA Product Code

• CEM: Electrode, Ion Specific, Potassium

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 [Potassium Electrode]

• 00811403015788: ME-2101D
• 00811403010127: Measuring concentration of Potassium in whole blood, serum, plasma, and diluted urine samples.
• 00811403018796: AW-903394D
• 00811403012558: BM-371038D
• 00811403011506: BK-669114D
• 00811403017065: OY-MU9195D
• 00811403013319: CD-476270D