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Avanos

FDA UDI

Class I (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
AVANOS FDA UDI
Generic Name
Heat/moisture exchanger, single-use FDA UDI
Device Name
1500 Heat and Moisture Exchanger FDA UDI
Model / Reference
93819 FDA UDI
Description
1500 Heat and Moisture Exchanger FDA UDI

Identifiers

Catalog Number
153 FDA UDI
Primary DI / UDI-DI
00609038938196 FDA UDI
FDA Product Code
BYD FDA UDI
GMDN Term
Heat/moisture exchanger, single-use 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Heat/moisture exchanger, single-use

Avanos by Avanos Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heat/moisture exchanger, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Avanos Medical, Inc.

Sources (1)

  • FDA UDI 4979d1eb-8b22-4aa8-bd3e-ace6b680c8b1 35 fields · synced Jun 9, 2026