eudamed_udi Primary ID: 05904507656232

1117 (UDI 05904507656232)

Manufactured by Przedsiębiorstwo Handlowo-Usługowe "Technomex" Sp. z o.o.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The 1117 (Model/Catalog Number: 01501409) is a medical device manufactured by Przedsiębiorstwo Handlowo-Usługowe "Technomex" Sp. z o.o.. This product is indexed under FDA Product Code / Category Classification Z120618 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 01501409
Product Code / EMDN: Z120618
Device Name: 1117
Database Sync Date: 2026-08-09 17:01:47

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 1117?

The registered manufacturer of record for 1117 is Przedsiębiorstwo Handlowo-Usługowe "Technomex" Sp. z o.o..

What is the Primary UDI-DI identifier for 1117?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904507656232.

What classification code is assigned to this device?

This device is registered under product classification code Z120618.

Similar Classification Devices (Z120618)

Other Devices by Przedsiębiorstwo Handlowo-Usługowe "Technomex" Sp. z o.o.

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