GPT /ALT (UDI 08034063843283)

Manufactured by FAR Srl

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

Scannable UDI-DI Representation

Device Regulatory Overview

The GPT /ALT (Model/Catalog Number: CL38-275) is a medical device manufactured by FAR Srl. This product is indexed under FDA Product Code / Category Classification W01010103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CL38-275
Product Code / EMDN: W01010103
Device Name: GPT / ALT
Database Sync Date: 2026-08-09 16:51:08

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 GPT /ALT?

The registered manufacturer of record for GPT /ALT is FAR Srl.

What is the Primary UDI-DI identifier for GPT /ALT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08034063843283.

What classification code is assigned to this device?

This device is registered under product classification code W01010103.

Similar Classification Devices (W01010103)

Other Devices by FAR Srl

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