eudamed_udi Primary ID: 08033638325377

SURTRON TOUCH HP 200 (UDI 08033638325377)

Manufactured by LED SpA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The SURTRON TOUCH HP 200 (Model/Catalog Number: 10100.T402) is a medical device manufactured by LED SpA. This product is indexed under FDA Product Code / Category Classification Z12010902 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 10100.T402
Product Code / EMDN: Z12010902
Device Name: SURTRON TOUCH HP 400
Database Sync Date: 2026-08-09 18:23:48

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 SURTRON TOUCH HP 200?

The registered manufacturer of record for SURTRON TOUCH HP 200 is LED SpA.

What is the Primary UDI-DI identifier for SURTRON TOUCH HP 200?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033638325377.

What classification code is assigned to this device?

This device is registered under product classification code Z12010902.

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