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Fisher & Paykel Healthcare

FDA UDI

Class I (US FDA UDI)

by Fisher & Paykel Healthcare, Inc.

Identity

Trade Name
Fisher & Paykel Healthcare FDA UDI
Generic Name
Oxygen low pressure hose FDA UDI
Device Name
Flow Diverter Adapter FDA UDI
Model / Reference
AA510J FDA UDI
Description
Flow Diverter Adapter FDA UDI

Identifiers

Primary DI / UDI-DI
09420012477743 FDA UDI
FDA Product Code
BYX FDA UDI
GMDN Term
Oxygen low pressure hose FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5860 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

Yes

FDA UDI

Category: Oxygen low pressure hose

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

Similar devices

Also classified as Oxygen low pressure hose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fisher & Paykel Healthcare, Inc.

Sources (1)

  • FDA UDI cef26b0a-1986-41f4-bec7-f5ab8e79ffbf 35 fields · synced Jun 8, 2026