gudid
Primary ID: M5005L4
Medichoice (UDI M5005L4)
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 M5005L4
Device Regulatory Overview
The Medichoice (Model/Catalog Number: M5005L4) is a medical device manufactured by OWENS & MINOR DISTRIBUTION, INC.. This product is indexed under FDA Product Code / Category Classification MUI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M5005L4
- Product Code / EMDN
- MUI
- Device Name
- Gel Ultrasound Standard 5 Liter Non-Sterile Fragrance Free Glacial Tint Not Made With Natural Rubber Latex MediChoice
- Database Sync Date
- 2026-08-09 09:16:25
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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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 M5005L4.
What classification code is assigned to this device?
This device is registered under product classification code MUI.
Similar Classification Devices (MUI)
Other Devices by OWENS & MINOR DISTRIBUTION, INC.
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