GUDIDData
eudamed_udi Primary ID: 04042301188670

LL 2012/6 Set m Y-Stück + 2. Leitung (UDI 04042301188670)

Manufactured by PFM medical mepro GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LL 2012/6 Set m Y-Stück + 2. Leitung - Primary ID 04042301188670

Device Regulatory Overview

The LL 2012/6 Set m Y-Stück + 2. Leitung (Model/Catalog Number: 73016) is a medical device manufactured by PFM medical mepro GmbH. This product is indexed under FDA Product Code / Category Classification A03040199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
73016
Product Code / EMDN
A03040199
Device Name
Infusionsset
Database Sync Date
2026-08-09 16:29:02

Full Regulatory Attributes

🔒 Token Gated
{
    "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 LL 2012/6 Set m Y-Stück + 2. Leitung?

The registered manufacturer of record for LL 2012/6 Set m Y-Stück + 2. Leitung is PFM medical mepro GmbH.

What is the Primary UDI-DI identifier for LL 2012/6 Set m Y-Stück + 2. Leitung?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04042301188670.

What classification code is assigned to this device?

This device is registered under product classification code A03040199.

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