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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, 14 ft, Standard, residential, hoistway by others, battery, indoor FDA UDI
Model / Reference
VPL FDA UDI
Description
Ameriglide, Platform lift, 14 ft, Standard, residential, hoistway by others, battery, indoor FDA UDI

Identifiers

Catalog Number
VPL1400ARADCI FDA UDI
Primary DI / UDI-DI
00817650025280 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

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Manufacturer

Manufacturer
Harmar Summit, LLC

Sources (1)

  • FDA UDI 7bf6e317-e17a-45d0-b584-8ad28f1c836c 35 fields · synced Jun 6, 2026