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SleepImage

FDA UDI

Class II (US FDA UDI)

by MyCardio, LLC

Identity

Trade Name
SleepImage FDA UDI
Generic Name
Multiple physiological signal amplifier FDA UDI
Device Name
Web based software FDA UDI
Model / Reference
8 FDA UDI
Description
Web based software FDA UDI

Identifiers

Primary DI / UDI-DI
B315SLEEPIMAGECOM0 FDA UDI
FDA Product Code
MNR FDA UDI
GMDN Term
Multiple physiological signal amplifier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2375 FDA UDI
Commercial Distribution
Not 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

No

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

SleepImage by MyCardio, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MyCardio, LLC

Sources (1)

  • FDA UDI 0ac776e3-3458-429f-a9b1-a71029bef014 34 fields · synced Jun 1, 2026