eudamed_udi Primary ID: 07290117812211

Hex Driver 2.5mm (UDI 07290117812211)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Hex Driver 2.5mm (Model/Catalog Number: 4152) is a medical device manufactured by Alpha Bio Tec Ltd.. This product is indexed under FDA Product Code / Category Classification L0318 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 4152
Product Code / EMDN: L0318
Device Name: Drivers
Database Sync Date: 2026-08-09 16:29:36

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 Hex Driver 2.5mm?

The registered manufacturer of record for Hex Driver 2.5mm is Alpha Bio Tec Ltd..

What is the Primary UDI-DI identifier for Hex Driver 2.5mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07290117812211.

What classification code is assigned to this device?

This device is registered under product classification code L0318.

Similar Classification Devices (L0318)

Other Devices by Alpha Bio Tec Ltd.

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