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Quickie 7 Series

FDA UDI

Class I (US FDA UDI)

by Sunrise Medical (US) LLC

Identity

Trade Name
Quickie 7 Series FDA UDI
Generic Name
Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible FDA UDI
Device Name
The QUICKIE® 7 Series redefines ultra lightweight wheelchair technology for the active user. Its personalized ergonomics, premium materials, and open back design offer you ultimate freedom of movement. Where will you go? FDA UDI
Model / Reference
7 FDA UDI
Description
The QUICKIE® 7 Series redefines ultra lightweight wheelchair technology for the active user. Its personalized ergonomics, premium materials, and open back design offer you ultimate freedom of movement. Where will you go? FDA UDI

Identifiers

Catalog Number
EIPW11 FDA UDI
Primary DI / UDI-DI
00016958052367 FDA UDI
FDA Product Code
IOR FDA UDI
GMDN Term
Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3850 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, occupant-driven, rear-wheels-operated, non-collapsible

Quickie 7 Series by Sunrise Medical (US) LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair, occupant-driven, rear-wheels-operated, non-collapsible.

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 1945414d-196a-46bc-87a4-34e45605dc46 34 fields · synced Jun 9, 2026