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Probasics

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
PROBASICS FDA UDI
Generic Name
Basic electric hospital bed FDA UDI
Device Name
Full Electric Bed 36 X 80, Springs, Motor, Hi/Low Shaft FDA UDI
Model / Reference
HBFESS FDA UDI
Description
Full Electric Bed 36 X 80, Springs, Motor, Hi/Low Shaft FDA UDI

Identifiers

Primary DI / UDI-DI
00815067072781 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

Yes

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: Basic electric hospital bed

Probasics by Compass Health Brands Corp. — 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

Sources (1)

  • FDA UDI f792f91f-77cd-4e3f-aa36-ba7c2da887c0 34 fields · synced May 30, 2026