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Wearable Patch

FDA UDI

Class I (US FDA UDI)

by Atlas Lift Tech, Inc.

Identity

Trade Name
Wearable Patch FDA UDI
Generic Name
Wearable multiple physiological parameter recorder, reusable FDA UDI
Device Name
A disposable patch that temporarily adheres to the patient’s sternum, allowing for the housing of the Atlas Sensor FDA UDI
Model / Reference
Rev A FDA UDI
Description
A disposable patch that temporarily adheres to the patient’s sternum, allowing for the housing of the Atlas Sensor FDA UDI

Identifiers

Primary DI / UDI-DI
00860008806017 FDA UDI
FDA Product Code
KMI FDA UDI
GMDN Term
Wearable multiple physiological parameter recorder, reusable 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Wearable multiple physiological parameter recorder, reusable

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

Similar devices

Also classified as Wearable multiple physiological parameter recorder, reusable.

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 a41d8fe7-6a3a-47f2-abf3-9d96f81cc1ff 33 fields · synced May 30, 2026