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Proning Accessory Kit

FDA UDI

Class II (US FDA UDI)

by Hill-Rom, Inc.

Identity

Trade Name
Proning Accessory Kit FDA UDI
Generic Name
Operating/examination/treatment table headrest, reusable FDA UDI
Device Name
PRONING ACCESSORY KIT FDA UDI
Model / Reference
P7529 FDA UDI
Description
PRONING ACCESSORY KIT FDA UDI

Identifiers

Primary DI / UDI-DI
00887761976726 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Operating/examination/treatment table headrest, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5100 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Operating/examination/treatment table headrest, reusable

Proning Accessory Kit by Hill-Rom, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating/examination/treatment table headrest, reusable.

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 c8566705-1bca-41f5-8d43-7e51223714ed 34 fields · synced May 30, 2026