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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
Heated respiratory humidifier FDA UDI
Device Name
Respiratory Humidifier FDA UDI
Model / Reference
950JUS FDA UDI
Description
Respiratory Humidifier FDA UDI

Identifiers

Catalog Number
950JUS FDA UDI
Primary DI / UDI-DI
09420012456625 FDA UDI
510(k) Number
K220703 FDA UDI
FDA Product Code
BTT FDA UDI
GMDN Term
Heated respiratory humidifier 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Heated respiratory humidifier

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 Heated respiratory humidifier.

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 f866a8b2-80ac-4b5b-869d-7752f407e5a1 37 fields · synced May 30, 2026