GUDIDData
eudamed_udi Primary ID: 05057881741916

MX PREMIUM UNIVERSAL DOUBLE PATELLA STRAP UNI S/M/L (UDI 05057881741916)

Manufactured by Medinox London Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MX PREMIUM UNIVERSAL DOUBLE PATELLA STRAP UNI S/M/L - Primary ID 05057881741916

Device Regulatory Overview

The MX PREMIUM UNIVERSAL DOUBLE PATELLA STRAP UNI S/M/L (Model/Catalog Number: MX74191) is a medical device manufactured by Medinox London Limited. This product is indexed under FDA Product Code / Category Classification M030402010103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MX74191
Product Code / EMDN
M030402010103
Device Name
STANDARD COMPRESSION SUPPORT WRAP
Database Sync Date
2026-08-09 16:29:03

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 MX PREMIUM UNIVERSAL DOUBLE PATELLA STRAP UNI S/M/L?

The registered manufacturer of record for MX PREMIUM UNIVERSAL DOUBLE PATELLA STRAP UNI S/M/L is Medinox London Limited.

What is the Primary UDI-DI identifier for MX PREMIUM UNIVERSAL DOUBLE PATELLA STRAP UNI S/M/L?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05057881741916.

What classification code is assigned to this device?

This device is registered under product classification code M030402010103.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint