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Accumax Quantum™Surface

FDA UDI

Class II (US FDA UDI)

by Hill-Rom, Inc.

Identity

Trade Name
Accumax Quantum™Surface FDA UDI
Generic Name
Alternating-pressure inflator FDA UDI
Device Name
Hospital Bed Surface FDA UDI
Model / Reference
PCU2 FDA UDI
Description
Hospital Bed Surface FDA UDI

Identifiers

Primary DI / UDI-DI
00887761001183 FDA UDI
FDA Product Code
IOQ FDA UDI
GMDN Term
Alternating-pressure inflator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5170 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Alternating-pressure inflator

Accumax Quantum™Surface by Hill-Rom, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Alternating-pressure inflator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hill-Rom, Inc.

Sources (1)

  • FDA UDI cbc396d4-83d5-4aaa-8cdc-1ebb96437f44 34 fields · synced Jun 8, 2026