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Pinnacle

FDA UDI

Class II (US FDA UDI)

by Harmar Summit, LLC

Identity

Trade Name
Pinnacle FDA UDI
Generic Name
Stairlift, chair FDA UDI
Device Name
Chassis Power W/O OBS Sensors FDA UDI
Model / Reference
Pinnacle, Rave, Leaf FDA UDI
Description
Chassis Power W/O OBS Sensors FDA UDI

Identifiers

Catalog Number
SSL1301 FDA UDI
Primary DI / UDI-DI
00817650026225 FDA UDI
FDA Product Code
PCD FDA UDI
GMDN Term
Stairlift, chair FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5150 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: Stairlift, chair

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

Similar devices

Also classified as Stairlift, chair.

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 d98ff78c-dbe8-4825-84d7-a0f474d89e19 35 fields · synced Jun 8, 2026