GUDIDData
eudamed_udi Primary ID: D-084360386736731HM

Ferritin control, 1 x 2 mL (UDI D-084360386736731HM)

Manufactured by Chronolab Systems, S.L.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ferritin control, 1 x 2 mL - Primary ID D-084360386736731HM

Device Regulatory Overview

The Ferritin control, 1 x 2 mL (Model/Catalog Number: 101-0474) is a medical device manufactured by Chronolab Systems, S.L.. This product is indexed under FDA Product Code / Category Classification W0102152003 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
101-0474
Product Code / EMDN
W0102152003
Device Name
Ferritin control, 1 x 2 mL
Database Sync Date
2026-08-09 16:50:46

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 Ferritin control, 1 x 2 mL?

The registered manufacturer of record for Ferritin control, 1 x 2 mL is Chronolab Systems, S.L..

What is the Primary UDI-DI identifier for Ferritin control, 1 x 2 mL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-084360386736731HM.

What classification code is assigned to this device?

This device is registered under product classification code W0102152003.

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