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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
Respiratory oxygen therapy system FDA UDI
Device Name
S/USE RESUS KIT W/O MASK (10) FDA UDI
Model / Reference
900RD010 FDA UDI
Description
S/USE RESUS KIT W/O MASK (10) FDA UDI

Identifiers

Primary DI / UDI-DI
09420012429933 FDA UDI
510(k) Number
K892885 FDA UDI
FDA Product Code
BTL FDA UDI
GMDN Term
Respiratory oxygen therapy system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5925 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: Respiratory oxygen therapy system

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 Respiratory oxygen therapy system.

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 7fbc2359-3430-4b9a-bdc3-814b42f973dc 35 fields · synced Jun 8, 2026