Hudson Rci

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name: HUDSON RCI FDA UDI
Generic Name: Ventilator breathing circuit, reusable FDA UDI
Device Name: DRI-TECH VENTILATOR ACCESSORY FDA UDI
Model / Reference: HUD900 FDA UDI
Description: DRI-TECH VENTILATOR ACCESSORY FDA UDI

Identifiers

Catalog Number: HUD900 FDA UDI
Primary DI / UDI-DI: 10197344043132 FDA UDI
510(k) Number: K234032 FDA UDI
FDA Product Code: BZE FDA UDI
GMDN Term: Ventilator breathing circuit, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5270 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Ventilator breathing circuit, reusable

Hudson Rci by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K234032 also covers:

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 II	Pending data

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Manufacturer

Manufacturer: Medline Industries, Inc.

Sources (1)

FDA UDI f742cf5b-726c-46d8-8c71-9b93fd3199b7 37 fields · synced May 31, 2026