MOBI

GUDID 10891040701111

Oral Digital Thermometer

MOBI TECHNOLOGIES, INC.

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• Primary Device ID: 10891040701111
• NIH Device Record Key: 9ebb7ce8-2fc1-4351-829d-abeec3f9712d
• Commercial Distribution Discontinuation: 2025-12-31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MOBI
• Version Model Number: 70111
• 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	00891040701114 [Primary]
GS1	10891040701111 [Package]; Contains: 00891040701114; Package: Cardboard [12 Units]; Discontinued: 2025-12-31; In Commercial Distribution
GS1	20891040701118 [Package]; Package: Cardboard [4 Units]; Discontinued: 2025-12-31; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101387

FDA Product Code

• FLL: Thermometer, Electronic, Clinical

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: 2020-05-15
• Device Publish Date: 2020-05-07

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• 20891040701187: MOBI Air Non-Contact Digital Thermometer
• 20891040701132: Non-Contact Thermometer
• 10891040701111: Oral Digital Thermometer
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• 20891040701217: Prime Ear and Forehead Thermometer.
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