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Twister

FDA UDI

Class I (US FDA UDI)

by Pride Mobility Products Corp.

Identity

Trade Name
TWISTER FDA UDI
Generic Name
Assistive input-control operation training device, selection techniques FDA UDI
Device Name
A device designed to assist a person with a disability in the techniques of selecting the correct input device in order to operate a connected primary device. FDA UDI
Model / Reference
TWISTER FDA UDI
Description
A device designed to assist a person with a disability in the techniques of selecting the correct input device in order to operate a connected primary device. FDA UDI

Identifiers

Catalog Number
N/A FDA UDI
Primary DI / UDI-DI
00606509900140 FDA UDI
FDA Product Code
KNO FDA UDI
GMDN Term
Assistive input-control operation training device, selection techniques FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3910 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assistive input-control operation training device, selection techniques

Twister by Pride Mobility Products Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assistive input-control operation training device, selection techniques.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pride Mobility Products Corp.

Sources (1)

  • FDA UDI 26e43472-b980-462e-a9ab-c5aa4da5b35a 34 fields · synced Jun 4, 2026