GUDIDData
eudamed_udi Primary ID: 08437023168332

CODO/TALON LUX STD (UDI 08437023168332)

Manufactured by EUROBASTON, S.L. - NIF B33851155

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CODO/TALON LUX STD - Primary ID 08437023168332

Device Regulatory Overview

The CODO/TALON LUX STD (Model/Catalog Number: 02701) is a medical device manufactured by EUROBASTON, S.L. - NIF B33851155. This product is indexed under FDA Product Code / Category Classification Y090612 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
02701
Product Code / EMDN
Y090612
Device Name
PROTECTOR
Database Sync Date
2026-08-09 17:27:14

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 CODO/TALON LUX STD?

The registered manufacturer of record for CODO/TALON LUX STD is EUROBASTON, S.L. - NIF B33851155.

What is the Primary UDI-DI identifier for CODO/TALON LUX STD?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437023168332.

What classification code is assigned to this device?

This device is registered under product classification code Y090612.

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