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Scout

FDA UDI

Class II (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
Scout FDA UDI
Generic Name
Assistive scooter, electric-motor-driven FDA UDI
Device Name
Scout 3-Wheel Scooter, Red/Blue FDA UDI
Model / Reference
RBSFSCOUT3 FDA UDI
Description
Scout 3-Wheel Scooter, Red/Blue FDA UDI

Identifiers

Primary DI / UDI-DI
00822383542744 FDA UDI
FDA Product Code
INI FDA UDI
GMDN Term
Assistive scooter, electric-motor-driven FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3800 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 74ed4f13-5ea8-4223-b53f-777299356c48 34 fields · synced Jun 8, 2026