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ARES Nasal Cannula

FDA UDI

Class II (US FDA UDI)

by WATERMARK MEDICAL Inc

Identity

Trade Name
ARES Nasal Cannula FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
ARES Nasal Cannula FDA UDI
Model / Reference
1130 FDA UDI
Description
ARES Nasal Cannula FDA UDI

Identifiers

Catalog Number
W19729 FDA UDI
Primary DI / UDI-DI
00854485007197 FDA UDI
FDA Product Code
NFB FDA UDI
GMDN Term
Nasal oxygen cannula, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nasal oxygen cannula, basic

ARES Nasal Cannula by WATERMARK MEDICAL Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal oxygen cannula, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a6f511b4-b306-43d4-972e-425973d89a06 35 fields · synced Jun 1, 2026