gudid Primary ID: PCIU-ARS2

DARCO PegContour Insole Uni (UDI PCIU-ARS2)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DARCO PegContour Insole Uni (Model/Catalog Number: PCIU-ARS2) is a medical device manufactured by Darco (Europe) GmbH. This product is indexed under FDA Product Code / Category Classification FMP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PCIU-ARS2
Product Code / EMDN: FMP
Device Name: M Grey/Blue for AllRound Shoe
Database Sync Date: 2026-08-09 09:17:36

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of DARCO PegContour Insole Uni?

The registered manufacturer of record for DARCO PegContour Insole Uni is Darco (Europe) GmbH.

What is the Primary UDI-DI identifier for DARCO PegContour Insole Uni?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PCIU-ARS2.

What classification code is assigned to this device?

This device is registered under product classification code FMP.

Similar Classification Devices (FMP)

Other Devices by Darco (Europe) GmbH

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint