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HUMIDAIRE 3i

FDA UDI

Class II (US FDA UDI)

by Resmed Corp

Identity

Trade Name
HUMIDAIRE 3i FDA UDI
Generic Name
Heated respiratory humidifier FDA UDI
Device Name
HUMIDAIRE 3i CLEANING PLUG PACK FDA UDI
Model / Reference
33947 FDA UDI
Description
HUMIDAIRE 3i CLEANING PLUG PACK FDA UDI

Identifiers

Catalog Number
33947 FDA UDI
Primary DI / UDI-DI
00619498339471 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
Heated respiratory humidifier FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 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

No

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

No

FDA UDI

Category: Heated respiratory humidifier

HUMIDAIRE 3i by Resmed Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heated respiratory humidifier.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Resmed Corp

Sources (1)

  • FDA UDI 09964956-eac0-4d4b-8030-a68165bb3721 36 fields · synced Jun 8, 2026