Sunbeam

GUDID 00694501169801

Deluxe Pulse Oximeter

Star Elite Inc

Pulse oximeter

• Primary Device ID: 00694501169801
• NIH Device Record Key: 023f7a66-4e7d-40ef-92a6-136c6fc49a5c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sunbeam
• Version Model Number: CMS50DA
• Company DUNS: 201197410
• Company Name: Star Elite Inc
• 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: false
• Serial Number: true
• Manufacturing Date: false
• 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	00694501169801 [Primary]

FDA Product Code

• OCH: Oximeter, Infrared, Sporting, Aviation

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: 2023-08-07
• Device Publish Date: 2023-07-28

On-Brand Devices [Sunbeam]

• 30694501169857: Upper arm blood pressure monitor intended for use in adults to measure heartbeat rate and blood
• 00694501169818: Wrist Cuff Blood Pressure Monitor
• 00694501169825: HW-F1
• 00694501169801: Deluxe Pulse Oximeter