← Back to catalogue

Drive

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
Drive FDA UDI
Generic Name
Patient transfer sliding board FDA UDI
Device Name
Part Patient Room Parts Product Description Armrest,D574,Jade,1/ea FDA UDI
Model / Reference
D574P-1070J FDA UDI
Description
Part Patient Room Parts Product Description Armrest,D574,Jade,1/ea FDA UDI

Identifiers

Primary DI / UDI-DI
00822383157801 FDA UDI
FDA Product Code
KMN FDA UDI
INN FDA UDI
GMDN Term
Patient transfer sliding board FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6140 FDA UDI
890.3100 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: Patient transfer sliding board

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

Similar devices

Also classified as Patient transfer sliding board.

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 577f7b08-c514-4af1-8fab-08a1be350741 33 fields · synced Jun 8, 2026