HG 100 Humidifier Guard

FDA UDI

Class I (US FDA UDI)

by Instrumentation Industries, Incorporated

Identity

Trade Name: HG 100 Humidifier Guard FDA UDI
Generic Name: Breathing circuit condensate trap, reusable FDA UDI
Device Name: The HG 100 Humidifier Guard is intended for use with a humidifier installed within a ventilator circuit. The device allows for safe removal of condensation and patient secretions that have accumulated in the inspiratory limb of a ventilator circuit. The HG100 protects the humidifier by allowing these liquids to be collected in the device and then to be easily removed by suction when necessary. FDA UDI
Model / Reference: HG 100 FDA UDI
Description: The HG 100 Humidifier Guard is intended for use with a humidifier installed within a ventilator circuit. The device allows for safe removal of condensation and patient secretions that have accumulated in the inspiratory limb of a ventilator circuit. The HG100 protects the humidifier by allowing these liquids to be collected in the device and then to be easily removed by suction when necessary. FDA UDI

Identifiers

Catalog Number: HG 100 FDA UDI
Primary DI / UDI-DI: M996HG1000 FDA UDI
FDA Product Code: BYH FDA UDI
GMDN Term: Breathing circuit condensate trap, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5995 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Hydrogen Peroxide FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Breathing circuit condensate trap, reusable

HG 100 Humidifier Guard by Instrumentation Industries, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Instrumentation Industries, Incorporated

Sources (1)

FDA UDI 5a6b5bf5-f5ab-4ef2-89e3-dfc1ff1fd2f8 35 fields · synced May 30, 2026