GUDIDData
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eudamed_udi Primary ID: 03663394002295

Axiom (UDI 03663394002295)

Manufactured by anthogyr

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Axiom - Primary ID 03663394002295

Device Regulatory Overview

The Axiom (Model/Catalog Number: OPTP240) 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
OPTP240
Product Code / EMDN
P010299
Device Name
Axiom 2.8 Abutment (PEEK)
Database Sync Date
2026-08-09 16:29:04

Full Regulatory Attributes

🔒 Token Gated 
{
    "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 03663394002295.

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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