eudamed_udi Primary ID: 08028718850542

GINOCCHIERA TUBOLARE/FORO TAGLIA XXL (UDI 08028718850542)

Manufactured by PAVIS SPA

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The GINOCCHIERA TUBOLARE/FORO TAGLIA XXL (Model/Catalog Number: 023BL XXL) 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: 023BL XXL
Product Code / EMDN: Y061209
Device Name: LINEA GAMBA GINOCCHIO
Database Sync Date: 2026-08-09 16:47:21

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 GINOCCHIERA TUBOLARE/FORO TAGLIA XXL?

The registered manufacturer of record for GINOCCHIERA TUBOLARE/FORO TAGLIA XXL is PAVIS SPA.

What is the Primary UDI-DI identifier for GINOCCHIERA TUBOLARE/FORO TAGLIA XXL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08028718850542.

What classification code is assigned to this device?

This device is registered under product classification code Y061209.

Similar Classification Devices (Y061209)

Other Devices by PAVIS SPA

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