MOBI

GUDID 10891040702033

Ultra Pulse Digital Thermometer

MOBI TECHNOLOGIES, INC.

Infrared patient thermometer, skin

• Primary Device ID: 10891040702033
• NIH Device Record Key: fa2f8327-be56-4b7a-bb72-e77489fba196
• Commercial Distribution Discontinuation: 2020-01-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MOBI
• Version Model Number: 70203
• 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

Customer Support Contacts

• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com
• Phone: 3239043000
• Email: Compliance@getmobi.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00891040702036 [Primary]
GS1	10891040702033 [Package]; Contains: 00891040702036; Package: Cardboard [3 Units]; Discontinued: 2020-01-01; Not in Commercial Distribution
GS1	20891040702030 [Package]; Package: Cardboard [4 Units]; Discontinued: 2018-05-25; Not in Commercial Distribution
GS1	30891040702037 [Package]; Contains: 00891040702036; Package: Cardboard [2 Units]; Discontinued: 2020-01-01; Not in Commercial Distribution
GS1	40891040702034 [Package]; Contains: 30891040702037; Package: Cardboard [6 Units]; Discontinued: 2020-01-01; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K100488

FDA Product Code

• FLL: Thermometer, Electronic, Clinical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 7
• Public Version Date: 2020-12-04
• Device Publish Date: 2017-02-11

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• 20891040701187: MOBI Air Non-Contact Digital Thermometer
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• 10891040702033: Ultra Pulse Digital Thermometer
• 20891040701217: Prime Ear and Forehead Thermometer.
• 20891040701200: Ultra Pulse Digital Thermometer
• 10891040701197: 70119
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