Rite365

GUDID 00860000362320

MAYBEAM LLC

Patient monitoring system module, blood pressure, noninvasive

• Primary Device ID: 00860000362320
• NIH Device Record Key: e474468e-4930-4b55-9f13-f241ae4c04eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rite365
• Version Model Number: Premium W4
• Company DUNS: 081556538
• Company Name: MAYBEAM LLC
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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	00860000362320 [Primary]

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

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: 2019-01-21
• Device Publish Date: 2018-12-20

On-Brand Devices [Rite365]

• 00860000362320: Premium W4
• 00860000362313: CB 15
• 00860000362306: Premium A1