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ARES COC Cable

FDA UDI

Class II (US FDA UDI)

by WATERMARK MEDICAL Inc

Identity

Trade Name
ARES COC Cable FDA UDI
Generic Name
Home-use sleep apnoea recording system FDA UDI
Device Name
ARES CoC Cable FDA UDI
Model / Reference
610/620 FDA UDI
Description
ARES CoC Cable FDA UDI

Identifiers

Catalog Number
W14205 FDA UDI
Primary DI / UDI-DI
00854485007142 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

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

Category: Home-use sleep apnoea recording system

ARES COC Cable 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

Manufacturer
WATERMARK MEDICAL Inc

Sources (1)

  • FDA UDI 728f0699-5626-479c-bf9b-d5151042f579 35 fields · synced Jun 8, 2026