← Back to catalogue

Stratos

FDA UDI

Class II (US FDA UDI)

by Harmar Summit, LLC

Identity

Trade Name
Stratos FDA UDI
Generic Name
Wheelchair/occupant lift FDA UDI
Device Name
Ameriglide, Platform lift, 4 ft, Standard, residential, hoistway, battery, indoor FDA UDI
Model / Reference
VPL FDA UDI
Description
Ameriglide, Platform lift, 4 ft, Standard, residential, hoistway, battery, indoor FDA UDI

Identifiers

Catalog Number
VPL0400ARWDCI FDA UDI
Primary DI / UDI-DI
00817650025433 FDA UDI
FDA Product Code
PCE FDA UDI
GMDN Term
Wheelchair/occupant 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

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

Yes

FDA UDI

Category: Wheelchair/occupant lift

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

Similar devices

Also classified as Wheelchair/occupant lift.

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

Manufacturer
Harmar Summit, LLC

Sources (1)

  • FDA UDI 89c136bd-b657-4458-be1d-475a898ed7bb 35 fields · synced May 31, 2026