← Back to catalogue

Drive

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
Drive FDA UDI
Generic Name
Bedrail FDA UDI
Device Name
BedsRails Product Description: Half Rail,T-Style,BrownVein,1pr/cs FDA UDI
Model / Reference
15021BV FDA UDI
Description
BedsRails Product Description: Half Rail,T-Style,BrownVein,1pr/cs FDA UDI

Identifiers

Primary DI / UDI-DI
00822383143361 FDA UDI
FDA Product Code
FNJ FDA UDI
GMDN Term
Bedrail FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5120 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: Bedrail

Drive by Drive Devilbiss Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bedrail.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Sources (1)

  • FDA UDI d125085e-8587-46a5-9064-14495d25f871 33 fields · synced Jun 8, 2026