pma Primary ID: P150011

Perceval PLUS Sutureless Heart Valve (UDI P150011)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Perceval PLUS Sutureless Heart Valve (Model/Catalog Number: Unspecified) is a medical device manufactured by Corcym S.r.l.. This product is indexed under FDA Product Code / Category Classification LWR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: N/A
Product Code / EMDN: LWR
Device Name: heart-valve, non-allograft tissue
Database Sync Date: 2026-08-09 10:04:44

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 Perceval PLUS Sutureless Heart Valve?

The registered manufacturer of record for Perceval PLUS Sutureless Heart Valve is Corcym S.r.l..

What is the Primary UDI-DI identifier for Perceval PLUS Sutureless Heart Valve?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P150011.

What classification code is assigned to this device?

This device is registered under product classification code LWR.

Similar Classification Devices (LWR)

Other Devices by Corcym S.r.l.

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