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Accora FloorBed

FDA UDI

Class II (US FDA UDI)

by Accora Inc

Identity

Trade Name
Accora FloorBed FDA UDI
Generic Name
Electrical assistive bed FDA UDI
Device Name
FloorBed 1 Plus, 4 Section Profiling Bed FDA UDI
Model / Reference
FloorBed 1 Plus FDA UDI
Description
FloorBed 1 Plus, 4 Section Profiling Bed FDA UDI

Identifiers

Catalog Number
NSB-0-FL5-200US FDA UDI
Primary DI / UDI-DI
05056147700063 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Electrical assistive 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrical assistive bed

Accora FloorBed by Accora Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical assistive bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Accora Inc

Sources (1)

  • FDA UDI 4cc5423c-85ff-4b72-9c9e-5e10cd8d3e90 35 fields · synced May 30, 2026