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ARES Secure Sleep Study Accessories

FDA UDI

Class II (US FDA UDI)

by WATERMARK MEDICAL Inc

Identity

Trade Name
ARES Secure Sleep Study Accessories FDA UDI
Generic Name
Home-use sleep apnoea recording system FDA UDI
Device Name
ARES Secure Sleep Study Accessories (Dongle and cable pack) FDA UDI
Model / Reference
610/620 FDA UDI
Description
ARES Secure Sleep Study Accessories (Dongle and cable pack) FDA UDI

Identifiers

Catalog Number
WM 1003 FDA UDI
Primary DI / UDI-DI
00854485007128 FDA UDI
FDA Product Code
MNR FDA UDI
GMDN Term
Home-use sleep apnoea recording system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.2375 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

Yes

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: Home-use sleep apnoea recording system

ARES Secure Sleep Study Accessories by WATERMARK MEDICAL Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Home-use sleep apnoea recording system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3a35dd33-5ed9-4305-88c0-33f8fef1fae5 36 fields · synced May 30, 2026