MOBI

GUDID 10891040702996

MOBI’s Fingertip Pulse Oximeter offers a noninvasive method for monitoring oxygen salutation. Though its reading of peripheral oxygen saturation (SPO2). It is portable, lightweight and multi-functional that can perform the measurement within 10 seconds.

MOBI TECHNOLOGIES, INC.

Pulse oximeter, line-powered

• Primary Device ID: 10891040702996
• NIH Device Record Key: 95a5f9e5-c2b3-4b3e-8e95-0b1615e431b4
• Commercial Distribution Discontinuation: 2025-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MOBI
• Version Model Number: 70299
• Company DUNS: 137468570
• Company Name: MOBI TECHNOLOGIES, 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: true
• Serial Number: false
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00891040702999 [Primary]
GS1	10891040702996 [Package]; Contains: 00891040702999; Package: Cardboard [6 Units]; Discontinued: 2025-12-31; In Commercial Distribution
GS1	20891040702993 [Package]; Package: Cardboard [4 Units]; Discontinued: 2025-12-31; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173123

FDA Product Code

• DQA: Oximeter

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: 2021-02-19
• Device Publish Date: 2021-02-11

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