P500 Surface

FDA UDI

Class II (US FDA UDI)

by Hill-Rom, Inc.

Identity

Trade Name: P500 Surface FDA UDI
Generic Name: Alternating-pressure inflator FDA UDI
Device Name: Hospital Bed Surface Controller FDA UDI
Model / Reference: P005723CAP02 FDA UDI
Description: Hospital Bed Surface Controller FDA UDI

Identifiers

Primary DI / UDI-DI: 00887761001015 FDA UDI
FDA Product Code: IOQ FDA UDI
FNL FDA UDI
GMDN Term: Alternating-pressure inflator FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5170 FDA UDI
880.5100 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

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Alternating-pressure inflator

P500 Surface by Hill-Rom, Inc. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Hill-Rom, Inc.

Sources (1)

FDA UDI 12e71a16-565f-4710-ae2c-b3379f68f703 34 fields · synced May 31, 2026