eudamed_udi Primary ID: 00607915138950

Alexis Orthopaedic Protector (UDI 00607915138950)

Manufactured by Applied Medical Resources Corporation

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Alexis Orthopaedic Protector (Model/Catalog Number: HR104) is a medical device manufactured by Applied Medical Resources Corporation. This product is indexed under FDA Product Code / Category Classification K01020106 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: HR104
Product Code / EMDN: K01020106
Device Name: Alexis® Orthopedic Protectors
Database Sync Date: 2026-08-09 16:47:25

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 Alexis Orthopaedic Protector?

The registered manufacturer of record for Alexis Orthopaedic Protector is Applied Medical Resources Corporation.

What is the Primary UDI-DI identifier for Alexis Orthopaedic Protector?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00607915138950.

What classification code is assigned to this device?

This device is registered under product classification code K01020106.

Similar Classification Devices (K01020106)

Other Devices by Applied Medical Resources Corporation

Programmatic Export

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

JSON API Endpoint