eudamed_udi Primary ID: 04007418600019

Pflastersortiment, DIN 13019 (UDI 04007418600019)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Pflastersortiment, DIN 13019 (Model/Catalog Number: 60001) is a medical device manufactured by Hans Hepp GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification M04010101,M04010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 60001
Product Code / EMDN: M04010101,M04010102
Device Name: Pflaster
Database Sync Date: 2026-08-09 16:45:37

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 Pflastersortiment, DIN 13019?

The registered manufacturer of record for Pflastersortiment, DIN 13019 is Hans Hepp GmbH & Co. KG.

What is the Primary UDI-DI identifier for Pflastersortiment, DIN 13019?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04007418600019.

What classification code is assigned to this device?

This device is registered under product classification code M04010101,M04010102.

Similar Classification Devices (M04010101,M04010102)

Other Devices by Hans Hepp GmbH & Co. KG

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