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Highlander

FDA UDI

Class II (US FDA UDI)

by Harmar Summit, LLC

Identity

Trade Name
HIGHLANDER FDA UDI
Generic Name
Assistive passenger lift FDA UDI
Device Name
COMMERCIAL PLATFORM LIFT, 400 STANDARD, DC, INSIDE FDA UDI
Model / Reference
CPL FDA UDI
Description
COMMERCIAL PLATFORM LIFT, 400 STANDARD, DC, INSIDE FDA UDI

Identifiers

Catalog Number
CPL0400SDCI FDA UDI
Primary DI / UDI-DI
00817650020131 FDA UDI
510(k) Number
K091881 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

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

Yes

FDA UDI

Category: Assistive passenger lift

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

Similar devices

Also classified as Assistive passenger lift.

Cleared under the same submission

K091881 also covers:

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 38d7552a-3ff6-4f9e-8516-fbb2ebe00899 36 fields · synced May 30, 2026