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MediChoice

FDA UDI

Class I (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
MediChoice FDA UDI
Generic Name
Wheelchair antitip device FDA UDI
Device Name
Wheelchair Rear Anti-Tippers Adjustable Position Fits All MediChoice Standard And Heavy-Duty Wheelchairs Reusable FDA UDI
Model / Reference
GEYATL FDA UDI
Description
Wheelchair Rear Anti-Tippers Adjustable Position Fits All MediChoice Standard And Heavy-Duty Wheelchairs Reusable FDA UDI

Identifiers

Primary DI / UDI-DI
10885632142581 FDA UDI
FDA Product Code
IML FDA UDI
GMDN Term
Wheelchair antitip device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Wheelchair antitip device

MediChoice by Owens & Minor Distribution, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair antitip device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 69164861-49f3-4cbf-a34f-d1a330664324 34 fields · synced Jun 6, 2026