GUDIDData
eudamed_udi Primary ID: 04270002229815

„Lisa“ von BECKER® (UDI 04270002229815)

Manufactured by Becker GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for „Lisa“ von BECKER® - Primary ID 04270002229815

Device Regulatory Overview

The „Lisa“ von BECKER® (Model/Catalog Number: 42 700022298LiegenFM) is a medical device manufactured by Becker GmbH. This product is indexed under FDA Product Code / Category Classification Y1803 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
42 700022298LiegenFM
Product Code / EMDN
Y1803
Device Name
„Lisa“ von BECKER® und „Pia“ von BECKER®
Database Sync Date
2026-08-09 17:03:29

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 „Lisa“ von BECKER®?

The registered manufacturer of record for „Lisa“ von BECKER® is Becker GmbH.

What is the Primary UDI-DI identifier for „Lisa“ von BECKER®?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04270002229815.

What classification code is assigned to this device?

This device is registered under product classification code Y1803.

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