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Ac611

FDA UDI

Class I (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
AC611 FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
AC611 High Flow Nasal Cannula, 22mm (M), Large, North America FDA UDI
Model / Reference
AC611 High Flow Nasal Cannula, 22mm (M), Large, NA FDA UDI
Description
AC611 High Flow Nasal Cannula, 22mm (M), Large, North America FDA UDI

Identifiers

Catalog Number
1134293 FDA UDI
Primary DI / UDI-DI
00606959047754 FDA UDI
FDA Product Code
CAT FDA UDI
GMDN Term
Nasal oxygen cannula, basic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5340 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasal oxygen cannula, basic

Ac611 by Respironics, Inc. — Class I — 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

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI ad276f7c-233e-4bdf-943a-8dc554e077b9 36 fields · synced May 30, 2026