Axiom (UDI 03663394873703)

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: TFLEX-N4-SAA) is a medical device manufactured by anthogyr. This product is indexed under FDA Product Code / Category Classification P010299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: TFLEX-N4-SAA
Product Code / EMDN: P010299
Device Name: Unitary Non-Sterile Abutment/Base/Coping (Titanium)
Database Sync Date: 2026-08-09 16:28:56

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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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 03663394873703.

What classification code is assigned to this device?

This device is registered under product classification code P010299.

Similar Classification Devices (P010299)

Other Devices by anthogyr

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