Experience Pod

FDA UDI

Class II (US FDA UDI)

by Hill-Rom, Inc.

Identity

Trade Name: Experience Pod FDA UDI
Generic Name: Nurse call system FDA UDI
Device Name: Experience Pod FDA UDI
Model / Reference: P7546A01 FDA UDI
Description: Experience Pod FDA UDI

Identifiers

Primary DI / UDI-DI: 00887761976542 FDA UDI
FDA Product Code: FNL FDA UDI
GMDN Term: Nurse call system 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

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

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Nurse call system

Experience Pod by Hill-Rom, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nurse call system.

WALL PLATE, RECEPTACLE — Crest Healthcare Supply · Class II
Smart Caregiver — Smart Caregiver Corporation · Class I
Fall Guardian — Smart Caregiver Corporation · Class I
Elite Infrared — Crest Healthcare Supply · Class II
CORRIDOR PILOT, 4 LAMP, 2 GANG — Crest Healthcare Supply · Class II
ProAlert 570 — JERON ELECTRONIC SYSTEMS INC · Class II
STATION, HELP, LIFELINE, 9171C — Crest Healthcare Supply · Class II
Excel Digital — Crest Healthcare Supply · Class II

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Hill-Rom, Inc.

Sources (1)

FDA UDI 4831cbf3-e4cf-417d-a0d4-520d40441872 35 fields · synced Jun 6, 2026