GUDIDData
eudamed_udi Primary ID: 06438129002485

evercare® inline DUOSET, 2-WAY, PVC Free, 180 cm (UDI 06438129002485)

Manufactured by OneMed Group Oy

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for evercare® inline DUOSET, 2-WAY, PVC Free, 180 cm - Primary ID 06438129002485

Device Regulatory Overview

The evercare® inline DUOSET, 2-WAY, PVC Free, 180 cm (Model/Catalog Number: 10576-01) is a medical device manufactured by OneMed Group Oy. This product is indexed under FDA Product Code / Category Classification A03010199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10576-01
Product Code / EMDN
A03010199
Device Name
Monosets
Database Sync Date
2026-08-09 16:44:51

Full Regulatory Attributes

🔒 Token Gated
{
    "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 evercare® inline DUOSET, 2-WAY, PVC Free, 180 cm?

The registered manufacturer of record for evercare® inline DUOSET, 2-WAY, PVC Free, 180 cm is OneMed Group Oy.

What is the Primary UDI-DI identifier for evercare® inline DUOSET, 2-WAY, PVC Free, 180 cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438129002485.

What classification code is assigned to this device?

This device is registered under product classification code A03010199.

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