GUDIDData
eudamed_udi Primary ID: 08056598552331

COLLARE EUSOFT RINFORZATO ZERO IMPACT MEDX ALTO CM8 EU8E MIS. S - CONF. DA 1 PZ. (UDI 08056598552331)

Manufactured by EUMEDICA SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for COLLARE EUSOFT RINFORZATO ZERO IMPACT MEDX ALTO CM8 EU8E MIS. S - CONF. DA 1 PZ. - Primary ID 08056598552331

Device Regulatory Overview

The COLLARE EUSOFT RINFORZATO ZERO IMPACT MEDX ALTO CM8 EU8E MIS. S - CONF. DA 1 PZ. (Model/Catalog Number: EU8ES) is a medical device manufactured by EUMEDICA SRL. This product is indexed under FDA Product Code / Category Classification Y060312 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
EU8ES
Product Code / EMDN
Y060312
Device Name
COLLARI
Database Sync Date
2026-08-09 16:48:40

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 COLLARE EUSOFT RINFORZATO ZERO IMPACT MEDX ALTO CM8 EU8E MIS. S - CONF. DA 1 PZ.?

The registered manufacturer of record for COLLARE EUSOFT RINFORZATO ZERO IMPACT MEDX ALTO CM8 EU8E MIS. S - CONF. DA 1 PZ. is EUMEDICA SRL.

What is the Primary UDI-DI identifier for COLLARE EUSOFT RINFORZATO ZERO IMPACT MEDX ALTO CM8 EU8E MIS. S - CONF. DA 1 PZ.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056598552331.

What classification code is assigned to this device?

This device is registered under product classification code Y060312.

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