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Quickie 500H

FDA UDI

Class II (US FDA UDI)

by Sunrise Medical (US) LLC

Identity

Trade Name
Quickie 500H FDA UDI
Generic Name
Wheelchair recliner, battery-powered FDA UDI
Device Name
The QUICKIE Q500 H brings you a unique blend of rear-wheel drive and mid-wheel drive technology, delivering impressive outdoor performance coupled with indoor maneuverability. Bringing you the best of both worlds and exceptional comfort. FDA UDI
Model / Reference
500H FDA UDI
Description
The QUICKIE Q500 H brings you a unique blend of rear-wheel drive and mid-wheel drive technology, delivering impressive outdoor performance coupled with indoor maneuverability. Bringing you the best of both worlds and exceptional comfort. FDA UDI

Identifiers

Primary DI / UDI-DI
00016958059847 FDA UDI
FDA Product Code
ITI FDA UDI
GMDN Term
Wheelchair recliner, battery-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3860 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

Yes

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: Wheelchair recliner, battery-powered

Quickie 500H by Sunrise Medical (US) LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair recliner, battery-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0e828b8c-04ea-45e7-80d9-05998a446393 33 fields · synced Jun 9, 2026