← Back to catalogue

Humidx Plus

FDA UDI

Class I (US FDA UDI)

by Resmed Pty Ltd

Identity

Trade Name
Humidx Plus FDA UDI
Generic Name
Heat/moisture exchanger insertable filter FDA UDI
Device Name
Humidx Plus 6PK FDA UDI
Model / Reference
38813 FDA UDI
Description
Humidx Plus 6PK FDA UDI

Identifiers

Primary DI / UDI-DI
00619498388134 FDA UDI
FDA Product Code
BYD FDA UDI
GMDN Term
Heat/moisture exchanger insertable filter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5375 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

No

FDA UDI

Category: Heat/moisture exchanger insertable filter

Humidx Plus by Resmed Pty Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heat/moisture exchanger insertable filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Resmed Pty Ltd

Sources (1)

  • FDA UDI a9fd37c7-67c1-4cdc-b68a-4f9f8d5d903d 34 fields · synced May 30, 2026