eudamed_udi Primary ID: 03663394006330

Anthofit (UDI 03663394006330)

Manufactured by anthogyr

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Anthofit (Model/Catalog Number: OIAN001) is a medical device manufactured by anthogyr. This product is indexed under FDA Product Code / Category Classification Q010207 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: OIAN001
Product Code / EMDN: Q010207
Device Name: Implant analog (HE-OI)
Database Sync Date: 2026-08-09 16:29:41

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 Anthofit?

The registered manufacturer of record for Anthofit is anthogyr.

What is the Primary UDI-DI identifier for Anthofit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03663394006330.

What classification code is assigned to this device?

This device is registered under product classification code Q010207.

Similar Classification Devices (Q010207)

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