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Sleep Apnea Feature

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref v 1.0Model Sleep Apnea-Android

by Samsung Electronics Co., Ltd.

Identity

Trade Name
Sleep Apnea Feature EUDAMED
Samsung Sleep Apnea Feature (Wear OS) FDA UDI
Generic Name
Patient general health self-management software FDA UDI
Device Name
Sleep Apnea Feature EUDAMED
The Sleep Apnea Feature is an over-the-counter (OTC) software-only, mobile medical application operating on a compatible Samsung Galaxy Watch and Phone. This feature is intended to detect signs of moderate to severe obstructive sleep apnea in the form of significant breathing disruptions in adult users 22 years and older, over a two-night monitoring period. This feature is intended for on-demand use. This feature is not intended for users who have previously been diagnosed with sleep apnea. Users should not use this feature to replace traditional methods of diagnosis and treatment by a qualified clinician. The data provided by this feature are also not intended to assist clinicians in diagnosing sleep disorders FDA UDI
Model / Reference
Sleep Apnea-Android EUDAMED
v 1.0 EUDAMED
1.X FDA UDI
Description
The Sleep Apnea Feature is an over-the-counter (OTC) software-only, mobile medical application operating on a compatible Samsung Galaxy Watch and Phone. This feature is intended to detect signs of moderate to severe obstructive sleep apnea in the form of significant breathing disruptions in adult users 22 years and older, over a two-night monitoring period. This feature is intended for on-demand use. This feature is not intended for users who have previously been diagnosed with sleep apnea. Users should not use this feature to replace traditional methods of diagnosis and treatment by a qualified clinician. The data provided by this feature are also not intended to assist clinicians in diagnosing sleep disorders FDA UDI

Identifiers

Primary DI / UDI-DI
08806094936872 EUDAMEDFDA UDI
Basic UDI-DI
8806094936896BY EUDAMED
510(k) Number
FDA Product Code
QZW FDA UDI
EMDN Code
Z12040182 GENERAL MEDICINE DIAGNOSIS AND MONITORING INSTRUMENTS - SOFTWARE ACCESSORIES EUDAMED
GMDN Term
Patient general health self-management software FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
868.2378 FDA UDI
Special Device Type
Software EUDAMED
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Sleep Apnea Feature by Samsung Electronics Co., Ltd — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
KR-MF-000023537
Authorised Representative
Samsung Electronics GmbH DE-AR-000007005

Sources (2)

  • EUDAMED f6df71fc-041b-460d-af19-477679e7cc01 61 fields · synced Jun 17, 2026
  • FDA UDI 0f91996b-0308-4489-9e34-a5f7afbb8756 34 fields · synced May 30, 2026