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Centrella™ Bed

FDA UDI

Class II (US FDA UDI)

by Hill-Rom, Inc.

Identity

Trade Name
Centrella™ Bed FDA UDI
Generic Name
Basic electric hospital bed FDA UDI
Device Name
Hospital Bed FDA UDI
Model / Reference
P7900B FDA UDI
Description
Hospital Bed FDA UDI

Identifiers

Primary DI / UDI-DI
00887761985162 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Basic electric hospital bed 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Basic electric hospital bed

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

Similar devices

Also classified as Basic electric hospital bed.

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 1c613f0b-4ce6-4e99-a069-96a1d76d9b99 34 fields · synced May 30, 2026