GUDIDData
eudamed_udi Primary ID: 08056598553338

WALKER ZERO IMPACT EU060B MODELLO BASSO MIS. M - CONF. DA 1 PZ (UDI 08056598553338)

Manufactured by EUMEDICA SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WALKER ZERO IMPACT EU060B MODELLO BASSO MIS. M - CONF. DA 1 PZ - Primary ID 08056598553338

Device Regulatory Overview

The WALKER ZERO IMPACT EU060B MODELLO BASSO MIS. M - CONF. DA 1 PZ (Model/Catalog Number: EU060BM) is a medical device manufactured by EUMEDICA SRL. This product is indexed under FDA Product Code / Category Classification Y06120601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
EU060BM
Product Code / EMDN
Y06120601
Device Name
WALKER
Database Sync Date
2026-08-09 16:46:55

Full Regulatory Attributes

πŸ”’ 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 WALKER ZERO IMPACT EU060B MODELLO BASSO MIS. M - CONF. DA 1 PZ?

The registered manufacturer of record for WALKER ZERO IMPACT EU060B MODELLO BASSO MIS. M - CONF. DA 1 PZ is EUMEDICA SRL.

What is the Primary UDI-DI identifier for WALKER ZERO IMPACT EU060B MODELLO BASSO MIS. M - CONF. DA 1 PZ?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056598553338.

What classification code is assigned to this device?

This device is registered under product classification code Y06120601.

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