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Wok

FDA UDI

Class I (US FDA UDI)

by Wheelchairs Of Kansas

Identity

Trade Name
WOK FDA UDI
Generic Name
Mobile bariatric examination/treatment chair, electric FDA UDI
Device Name
32" 230V Shuttle Series B -Advanced FDA UDI
Model / Reference
31060000 230v FDA UDI
Description
32" 230V Shuttle Series B -Advanced FDA UDI

Identifiers

Primary DI / UDI-DI
00845699004713 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Mobile bariatric examination/treatment chair, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 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

No

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: Mobile bariatric examination/treatment chair, electric

Wok by Wheelchairs Of Kansas — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mobile bariatric examination/treatment chair, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wheelchairs Of Kansas

Sources (1)

  • FDA UDI ce44d629-5dc2-4f10-abd3-90549ee0c1f8 33 fields · synced Jun 8, 2026