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Lumex

FDA UDI

Class I (US FDA UDI)

by GF Health Products, Inc

Identity

Trade Name
LUMEX FDA UDI
Generic Name
Walker tray FDA UDI
Device Name
WALKER BASKET FDA UDI
Model / Reference
603904A FDA UDI
Description
WALKER BASKET FDA UDI

Identifiers

Catalog Number
603904A FDA UDI
Primary DI / UDI-DI
M368603904A1 FDA UDI
FDA Product Code
INB FDA UDI
GMDN Term
Walker tray 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Walker tray

Lumex by GF Health Products, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Walker tray.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3bb7d5e8-74d9-4af0-8d22-3d9ef595660d 35 fields · synced May 30, 2026