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Mobi

FDA UDI

Class II (US FDA UDI)

by Mobi Technologies, Inc.

Identity

Trade Name
MOBI FDA UDI
Generic Name
General-purpose patient temperature probe, single-use FDA UDI
Device Name
Oral Digital Thermometer FDA UDI
Model / Reference
70111 FDA UDI
Description
Oral Digital Thermometer FDA UDI

Identifiers

Primary DI / UDI-DI
00891040701114 FDA UDI
510(k) Number
K101387 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
General-purpose patient temperature probe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose patient temperature probe, single-use

Mobi by Mobi Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose patient temperature probe, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9ebb7ce8-2fc1-4351-829d-abeec3f9712d 35 fields · synced Jun 1, 2026