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TransMotionMedical

FDA UDI

Class II (US FDA UDI)

by Winco Mfg., Llc

Identity

Trade Name
TransMotionMedical FDA UDI
Generic Name
Mobile bariatric examination/treatment chair, electric FDA UDI
Device Name
Stretcher, Wheeled, Powered, 750lb Max FDA UDI
Model / Reference
S750 FDA UDI
Description
Stretcher, Wheeled, Powered, 750lb Max FDA UDI

Identifiers

Primary DI / UDI-DI
00855630004054 FDA UDI
510(k) Number
K110671 FDA UDI
FDA Product Code
INK FDA UDI
GMDN Term
Mobile bariatric examination/treatment chair, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3690 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

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: Mobile bariatric examination/treatment chair, electric

TransMotionMedical by Winco Mfg., Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

K110671 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Winco Mfg., Llc

Sources (1)

  • FDA UDI 90de6e34-0a0f-4ec2-8d01-8bba24b2adec 35 fields · synced May 30, 2026