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Fisher & Paykel Healthcare

FDA UDI

Class II (US FDA UDI)

by Fisher & Paykel Healthcare, Inc.

Identity

Trade Name
Fisher & Paykel Healthcare FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
Optiflow Nasal Filtered Interface with CO2 Sampling Small FDA UDI
Model / Reference
AA031JS FDA UDI
Description
Optiflow Nasal Filtered Interface with CO2 Sampling Small FDA UDI

Identifiers

Catalog Number
AA031JS FDA UDI
Primary DI / UDI-DI
09420012470928 FDA UDI
510(k) Number
K201723 FDA UDI
FDA Product Code
BTT FDA UDI
GMDN Term
Nasal oxygen cannula, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5450 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Nasal oxygen cannula, basic

Fisher & Paykel Healthcare by Fisher & Paykel Healthcare, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal oxygen cannula, basic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5bd3fb71-3c8b-4b72-ad9b-dc6f01e5244f 38 fields · synced May 30, 2026