FREEDOM (UDI FREEDOM)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The FREEDOM (Model/Catalog Number: FREEDOM) is a medical device manufactured by EPTAMED SRL. This product is indexed under FDA Product Code / Category Classification KMY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: FREEDOM
Product Code / EMDN: KMY
Device Name: Preformed orthodontic tooth positioner
Database Sync Date: 2026-08-09 09:00:28

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 FREEDOM?

The registered manufacturer of record for FREEDOM is EPTAMED SRL.

What is the Primary UDI-DI identifier for FREEDOM?

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

What classification code is assigned to this device?

This device is registered under product classification code KMY.

Similar Classification Devices (KMY)

Other Devices by EPTAMED SRL

Programmatic Export

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

JSON API Endpoint