GUDIDData
eudamed_udi Primary ID: 08028718315713

TUTORE X INSTABILITA' LCA-LCP E LCM-LCL TAGLIA M SINISTRA (UDI 08028718315713)

Manufactured by PAVIS SPA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TUTORE X INSTABILITA' LCA-LCP E LCM-LCL TAGLIA M SINISTRA - Primary ID 08028718315713

Device Regulatory Overview

The TUTORE X INSTABILITA' LCA-LCP E LCM-LCL TAGLIA M SINISTRA (Model/Catalog Number: 053NE M SX) is a medical device manufactured by PAVIS SPA. This product is indexed under FDA Product Code / Category Classification Y061209 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
053NE M SX
Product Code / EMDN
Y061209
Device Name
LINEA GAMBA GINOCCHIO
Database Sync Date
2026-08-09 16:51:15

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 TUTORE X INSTABILITA' LCA-LCP E LCM-LCL TAGLIA M SINISTRA?

The registered manufacturer of record for TUTORE X INSTABILITA' LCA-LCP E LCM-LCL TAGLIA M SINISTRA is PAVIS SPA.

What is the Primary UDI-DI identifier for TUTORE X INSTABILITA' LCA-LCP E LCM-LCL TAGLIA M SINISTRA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08028718315713.

What classification code is assigned to this device?

This device is registered under product classification code Y061209.

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