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Freerider

FDA UDI

Class II (US FDA UDI)

by Freerider Corporation

Identity

Trade Name
FREERIDER FDA UDI
Generic Name
Assistive scooter, electric-motor-driven FDA UDI
Device Name
Vehicle FDA UDI
Model / Reference
FR1GDX FDA UDI
Description
Vehicle FDA UDI

Identifiers

Primary DI / UDI-DI
04713072966049 FDA UDI
510(k) Number
K133187 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
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Category: Assistive scooter, electric-motor-driven

Freerider by Freerider Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assistive scooter, electric-motor-driven.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b8b4d5be-d8ae-4e4c-9f04-4742962e7047 34 fields · synced Jun 6, 2026