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Switch-It

FDA UDI

Class I (US FDA UDI)

by Sunrise Medical (US) LLC

Identity

Trade Name
Switch-It FDA UDI
Generic Name
Wheelchair steering/control unit FDA UDI
Device Name
Alternative drive controls for users who cannot use standard power wheelchair controls. FDA UDI
Model / Reference
MicroGuide, MicroPilot, VersaGuide, VersaGuideEZ, Cool Cube FDA UDI
Description
Alternative drive controls for users who cannot use standard power wheelchair controls. FDA UDI

Identifiers

Catalog Number
SWI FDA UDI
Primary DI / UDI-DI
00016958058451 FDA UDI
FDA Product Code
KNO FDA UDI
GMDN Term
Wheelchair steering/control unit 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

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

Yes

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 steering/control unit

Switch-It by Sunrise Medical (US) LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair steering/control unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3fd0485b-eb9a-492c-a3f5-82ca2d7b25c4 34 fields · synced Jun 9, 2026