gudid
Primary ID: LGHT7503
MediChoice (UDI LGHT7503)
Manufactured by OWENS & MINOR DISTRIBUTION, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MediChoice - Primary ID LGHT7503
Device Regulatory Overview
The MediChoice (Model/Catalog Number: LGHT7503) is a medical device manufactured by OWENS & MINOR DISTRIBUTION, INC.. This product is indexed under FDA Product Code / Category Classification KZF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LGHT7503
- Product Code / EMDN
- KZF
- Device Name
- Light Examination 12 Inch Flexible Gooseneck Chrome-Plated With 60 Watt Bulb Not Made With Natural Rubber Latex MediChoice
- Database Sync Date
- 2026-08-09 09:16:25
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MediChoice?
The registered manufacturer of record for MediChoice is OWENS & MINOR DISTRIBUTION, INC..
What is the Primary UDI-DI identifier for MediChoice?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is LGHT7503.
What classification code is assigned to this device?
This device is registered under product classification code KZF.
Similar Classification Devices (KZF)
Other Devices by OWENS & MINOR DISTRIBUTION, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint