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Quickie 200R

FDA UDI

Class II (US FDA UDI)

by Sunrise Medical (US) LLC

Identity

Trade Name
Quickie 200R FDA UDI
Generic Name
Wheelchair recliner, battery-powered FDA UDI
Device Name
Ultra-compact RWD power wheelchair with super-tight indoor maneuverability and ZERO compromise on outdoor stability and performance. FDA UDI
Model / Reference
200R FDA UDI
Description
Ultra-compact RWD power wheelchair with super-tight indoor maneuverability and ZERO compromise on outdoor stability and performance. FDA UDI

Identifiers

Catalog Number
EIPW35 FDA UDI
Primary DI / UDI-DI
00016958058680 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 200R 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

Manufacturer
Sunrise Medical (US) LLC

Sources (1)

  • FDA UDI 2fa4f90a-bd36-41cc-912f-c7986731ab37 34 fields · synced Jun 9, 2026