eudamed_udi Primary ID: 03663394482653

Axiom (UDI 03663394482653)

Manufactured by anthogyr

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Axiom (Model/Catalog Number: OPFF45) is a medical device manufactured by anthogyr. This product is indexed under FDA Product Code / Category Classification L159099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: OPFF45
Product Code / EMDN: L159099
Device Name: Implant bed preparation instrument
Database Sync Date: 2026-08-09 16:30:10

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 Axiom?

The registered manufacturer of record for Axiom is anthogyr.

What is the Primary UDI-DI identifier for Axiom?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03663394482653.

What classification code is assigned to this device?

This device is registered under product classification code L159099.

Similar Classification Devices (L159099)

Other Devices by anthogyr

Programmatic Export

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

JSON API Endpoint