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RespVent™

FDA UDI

Class I (US FDA UDI)

by Cutting Edge Hc Brands Llc

Identity

Trade Name
RespVent™ FDA UDI
Generic Name
Heat/moisture exchanger, single-use FDA UDI
Device Name
RespVent Tracheostomy T- HME with Front Oxygen Port is a single use heat and moisture exchanger which transfers heat and humidity from the gas expired by the patient to the inspired gases. RespVent Trach T-HME is intended for use on patients who are breathing spontaneously through a tracheostomy tube. FDA UDI
Model / Reference
RTG-01052 FDA UDI
Description
RespVent Tracheostomy T- HME with Front Oxygen Port is a single use heat and moisture exchanger which transfers heat and humidity from the gas expired by the patient to the inspired gases. RespVent Trach T-HME is intended for use on patients who are breathing spontaneously through a tracheostomy tube. FDA UDI

Identifiers

Catalog Number
RTG-01052 FDA UDI
Primary DI / UDI-DI
00850108006080 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

RespVent™ by Cutting Edge Hc Brands Llc — 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 83509f41-bae0-4bd2-8fdf-d27581487c84 36 fields · synced Jun 8, 2026