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Atlas Sensor

FDA UDI

Class I (US FDA UDI)

by Atlas Lift Tech, Inc.

Identity

Trade Name
Atlas Sensor FDA UDI
Generic Name
Wireless patient monitor/sensor reporting software, professional-only FDA UDI
Device Name
A reusable, wireless, Bluetooth device that sends patient body orientation and movement information to the Bedside Mobility Monitor (BMM) that is housed within the Atlas Wearable Patch. FDA UDI
Model / Reference
Rev A FDA UDI
Description
A reusable, wireless, Bluetooth device that sends patient body orientation and movement information to the Bedside Mobility Monitor (BMM) that is housed within the Atlas Wearable Patch. FDA UDI

Identifiers

Primary DI / UDI-DI
00860008806024 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Wireless patient monitor/sensor reporting software, professional-only FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2400 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Wireless patient monitor/sensor reporting software, professional-only

Atlas Sensor by Atlas Lift Tech, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wireless patient monitor/sensor reporting software, professional-only.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Atlas Lift Tech, Inc.

Sources (1)

  • FDA UDI 3b520ca9-9c06-49ac-905e-0b5d1257db6f 33 fields · synced May 30, 2026