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Maximus System

FDA UDI

Class II (US FDA UDI)

by Hill-Rom Services Pte. Ltd.

Identity

Trade Name
Maximus System FDA UDI
Generic Name
In-exsufflation/lung-oscillation airway secretion-clearing system FDA UDI
Device Name
MAXIMUS SYSTEM, AC IRELAND FDA UDI
Model / Reference
POPT1ACIE FDA UDI
Description
MAXIMUS SYSTEM, AC IRELAND FDA UDI

Identifiers

Primary DI / UDI-DI
00887761975590 FDA UDI
FDA Product Code
NHJ FDA UDI
GMDN Term
In-exsufflation/lung-oscillation airway secretion-clearing system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 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

No

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
MRI Safety
MR Unsafe FDA UDI

Category: In-exsufflation/lung-oscillation airway secretion-clearing system

Maximus System by Hill-Rom Services Pte. Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as In-exsufflation/lung-oscillation airway secretion-clearing system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hill-Rom Services Pte. Ltd.

Sources (1)

  • FDA UDI 1817020e-422a-47f9-9325-238391115bff 34 fields · synced May 30, 2026