Sunbeam

GUDID 06945040105800

Fingertip Pulse Oximeter

Contec Medical Systems Co., Ltd.

Pulse oximeter, battery-powered

• Primary Device ID: 06945040105800
• NIH Device Record Key: b4eb807b-ff21-4859-a4e3-85a16026fe1d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sunbeam
• Version Model Number: CMS50DL
• Company DUNS: 529606295
• Company Name: Contec Medical Systems Co., Ltd.
• 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: 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	06945040105800 [Primary]
GS1	16945040105807 [Package]; Package: Carton [24 Units]; In Commercial Distribution

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: 2021-06-18
• Device Publish Date: 2021-06-10

On-Brand Devices [Sunbeam]

• 06945040105817: Fingertip Pulse Oximeter
• 06945040105800: Fingertip Pulse Oximeter