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inCourage®

FDA UDI

Class II (US FDA UDI)

by Respiratory Technologies, Inc.

Identity

Trade Name
inCourage® FDA UDI
Generic Name
Chest-oscillation airway secretion-clearing system generator FDA UDI
Device Name
Pulsating Therapy Unit FDA UDI
Model / Reference
ICS-1M-US-B FDA UDI
Description
Pulsating Therapy Unit FDA UDI

Identifiers

Primary DI / UDI-DI
00841561102808 FDA UDI
FDA Product Code
BYI FDA UDI
GMDN Term
Chest-oscillation airway secretion-clearing system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5665 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Chest-oscillation airway secretion-clearing system generator

inCourage® by Respiratory Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chest-oscillation airway secretion-clearing system generator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Respiratory Technologies, Inc.

Sources (1)

  • FDA UDI 0ddf203d-a17d-45dd-832f-956da82684e8 35 fields · synced Jun 8, 2026