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Heat Moisture Exchanger

FDA UDI

Class I (US FDA UDI)

by SUNSET HEALTHCARE SOLUTIONS, Inc.

Identity

Trade Name
Heat Moisture Exchanger FDA UDI
Generic Name
Heat/moisture exchanger, single-use FDA UDI
Device Name
Sunset Adult In-line Large Volume HME with Gas Sampling Port FDA UDI
Model / Reference
RES027ILLV FDA UDI
Description
Sunset Adult In-line Large Volume HME with Gas Sampling Port FDA UDI

Identifiers

Primary DI / UDI-DI
00848530107284 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

Yes

FDA UDI

Category: Heat/moisture exchanger, single-use

Heat Moisture Exchanger by SUNSET HEALTHCARE SOLUTIONS, 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

Sources (1)

  • FDA UDI e28703a6-77cd-4d1b-b037-88b15084200f 34 fields · synced May 30, 2026