GUDIDData
eudamed_udi Primary ID: 08056600607219

STRUMENTO PER COMPOSITO BS1 TITANIO (UDI 08056600607219)

Manufactured by MEDESY srl

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STRUMENTO PER COMPOSITO BS1 TITANIO - Primary ID 08056600607219

Device Regulatory Overview

The STRUMENTO PER COMPOSITO BS1 TITANIO (Model/Catalog Number: 494/1T) is a medical device manufactured by MEDESY srl. This product is indexed under FDA Product Code / Category Classification L159013 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
494/1T
Product Code / EMDN
L159013
Device Name
STRUMENTI CHIRURGICI RIUTILIZZABILI
Database Sync Date
2026-08-09 16:47:27

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 STRUMENTO PER COMPOSITO BS1 TITANIO?

The registered manufacturer of record for STRUMENTO PER COMPOSITO BS1 TITANIO is MEDESY srl.

What is the Primary UDI-DI identifier for STRUMENTO PER COMPOSITO BS1 TITANIO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056600607219.

What classification code is assigned to this device?

This device is registered under product classification code L159013.

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