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Wheelchair Powered

FDA UDI

Class II (US FDA UDI)

by Golden Brothers, Inc

Identity

Trade Name
WHEELCHAIR POWERED FDA UDI
Generic Name
Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible FDA UDI
Device Name
Battery powered wheelchair FDA UDI
Model / Reference
GP208 FDA UDI
Description
Battery powered wheelchair FDA UDI

Identifiers

Catalog Number
GP208 FDA UDI
Primary DI / UDI-DI
B247GP208 FDA UDI
510(k) Number
K011153 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

Yes

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

Wheelchair Powered by Golden Brothers, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 496c206f-2577-412a-939e-64cd668d7525 36 fields · synced Jun 8, 2026