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HumidX

FDA UDI

Class I (US FDA UDI)

by Resmed Corp

Identity

Trade Name
HumidX FDA UDI
Generic Name
Heat/moisture exchanger insertable filter FDA UDI
Device Name
Pack of 50 FDA UDI
Model / Reference
38808 FDA UDI
Description
Pack of 50 FDA UDI

Identifiers

Primary DI / UDI-DI
00619498388080 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

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

No

FDA UDI

Category: Heat/moisture exchanger insertable filter

HumidX by Resmed Corp — 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

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Manufacturer

Manufacturer
Resmed Corp

Sources (1)

  • FDA UDI 1d079301-a0b0-4da5-a513-14e1bdae1c01 34 fields · synced Jun 8, 2026