eudamed_udi Primary ID: 08426680716413

Pañal de Ferrara (UDI 08426680716413)

Manufactured by PRIM, S.A.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Pañal de Ferrara (Model/Catalog Number: F01 S) is a medical device manufactured by PRIM, S.A.. This product is indexed under FDA Product Code / Category Classification Y061215 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: F01 S
Product Code / EMDN: Y061215
Device Name: Ortesis de Cadera
Database Sync Date: 2026-08-09 16:29:31

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 Pañal de Ferrara?

The registered manufacturer of record for Pañal de Ferrara is PRIM, S.A..

What is the Primary UDI-DI identifier for Pañal de Ferrara?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08426680716413.

What classification code is assigned to this device?

This device is registered under product classification code Y061215.

Similar Classification Devices (Y061215)

Other Devices by PRIM, S.A.

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