Potassium Electrode

GUDID 04987762129865

JEOL LTD.

Potassium (K+) electrode IVD

• Primary Device ID: 04987762129865
• NIH Device Record Key: 483684b6-4992-4edf-b89c-043745618759
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Potassium Electrode
• Version Model Number: 781611385
• Company DUNS: 690565023
• Company Name: JEOL LTD.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04987762129865 [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: 2020-09-23
• Device Publish Date: 2020-09-15

Devices Manufactured by JEOL LTD.

• 04987762129759 - ISE Buffer (IS): 2020-10-19
• 04987762129766 - Reagent Probe S: 2020-09-23
• 04987762129773 - Reagent Probe Wash K: 2020-09-23
• 04987762129780 - Reagent Probe Wash 2: 2020-09-23
• 04987762129797 - Reagent Probe Wash 1: 2020-09-23
• 04987762129803 - Lamp Coolant C: 2020-09-23
• 04987762129810 - Cuvette Conditioner EX: 2020-09-23
• 04987762129827 - Cuvette Wash Solution 7: 2020-09-23