eudamed_udi Primary ID: 03663394484978

INTEGRAL (UDI 03663394484978)

Manufactured by anthogyr

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

Scannable UDI-DI Representation

Device Regulatory Overview

The INTEGRAL (Model/Catalog Number: GMVG42S) 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: GMVG42S
Product Code / EMDN: L159099
Device Name: Torque instrument (mandrel, mandrel extension) - class IIa
Database Sync Date: 2026-08-09 16:29:11

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 INTEGRAL?

The registered manufacturer of record for INTEGRAL is anthogyr.

What is the Primary UDI-DI identifier for INTEGRAL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03663394484978.

What classification code is assigned to this device?

This device is registered under product classification code L159099.

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