eudamed_udi Primary ID: 08028718797717

HUM-POLS CORTA DX M (UDI 08028718797717)

Manufactured by PAVIS SPA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The HUM-POLS CORTA DX M (Model/Catalog Number: 8003 DX M) is a medical device manufactured by PAVIS SPA. This product is indexed under FDA Product Code / Category Classification Y060612 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 8003 DX M
Product Code / EMDN: Y060612
Device Name: LINEA MANO BRACCIO POLSO
Database Sync Date: 2026-08-09 16:29:10

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 HUM-POLS CORTA DX M?

The registered manufacturer of record for HUM-POLS CORTA DX M is PAVIS SPA.

What is the Primary UDI-DI identifier for HUM-POLS CORTA DX M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08028718797717.

What classification code is assigned to this device?

This device is registered under product classification code Y060612.

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