eudamed_udi Primary ID: 08434048105151

Muslera Elástica AQTIVO Sport (UDI 08434048105151)

Manufactured by PRIM, S.A.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Muslera Elástica AQTIVO Sport (Model/Catalog Number: P709 L) is a medical device manufactured by PRIM, S.A.. This product is indexed under FDA Product Code / Category Classification Y061217 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: P709 L
Product Code / EMDN: Y061217
Device Name: Ortesis Femorales
Database Sync Date: 2026-08-09 17:13:41

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 Muslera Elástica AQTIVO Sport?

The registered manufacturer of record for Muslera Elástica AQTIVO Sport is PRIM, S.A..

What is the Primary UDI-DI identifier for Muslera Elástica AQTIVO Sport?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08434048105151.

What classification code is assigned to this device?

This device is registered under product classification code Y061217.

Similar Classification Devices (Y061217)

Other Devices by PRIM, S.A.

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