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Freedom Easy Ride

FDA UDI

Class II (US FDA UDI)

by Harmar Summit, LLC

Identity

Trade Name
FREEDOM EASY RIDE FDA UDI
Generic Name
Assistive passenger lift FDA UDI
Device Name
FREEDOM RESIDENTIAL PLATFORM LIFT, 400 STANDARD, AC, INSIDE FDA UDI
Model / Reference
RPL FDA UDI
Description
FREEDOM RESIDENTIAL PLATFORM LIFT, 400 STANDARD, AC, INSIDE FDA UDI

Identifiers

Catalog Number
FLR0400SACI FDA UDI
Primary DI / UDI-DI
00817650022890 FDA UDI
FDA Product Code
ING FDA UDI
GMDN Term
Assistive passenger lift FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3930 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

Yes

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

Yes

FDA UDI

Category: Assistive passenger lift

Freedom Easy Ride by Harmar Summit, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assistive passenger lift.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Harmar Summit, LLC

Sources (1)

  • FDA UDI a53b7e11-951a-4cca-806b-50a4c5b93211 35 fields · synced May 30, 2026