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Drive

FDA UDI

Class II (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
Drive FDA UDI
Generic Name
Basic electric home bed FDA UDI
Device Name
BedsSemi Product Description: CompetII HiLoHgtAdjBedw/HRail,FMatt,1/c FDA UDI
Model / Reference
15571HR-PKG-FM FDA UDI
Description
BedsSemi Product Description: CompetII HiLoHgtAdjBedw/HRail,FMatt,1/c FDA UDI

Identifiers

Primary DI / UDI-DI
00822383963693 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Basic electric home 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: Basic electric home bedElectrical assistive bed

Drive by Drive Devilbiss Healthcare — 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

Sources (1)

  • FDA UDI 639f3282-7ca1-4bda-9d9c-a49933bc5447 33 fields · synced Jun 8, 2026