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Quickie® Rear Wheel Drive Power Wheelchair

FDA UDI

Class II (US FDA UDI)

by Sunrise Medical (US) LLC

Identity

Trade Name
Quickie® Rear Wheel Drive Power Wheelchair FDA UDI
Generic Name
Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible FDA UDI
Device Name
S-6 Series Power Wheelchair FDA UDI
Model / Reference
EIS62 FDA UDI
Description
S-6 Series Power Wheelchair FDA UDI

Identifiers

Catalog Number
EIS62 FDA UDI
Primary DI / UDI-DI
05022408044252 FDA UDI
FDA Product Code
ITI FDA UDI
GMDN Term
Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3860 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Quickie® Rear Wheel Drive Power Wheelchair by Sunrise Medical (US) LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1d4dfef1-b395-45f8-81fc-e3c18532a9ea 36 fields · synced Jun 9, 2026