GUDIDData
eudamed_udi Primary ID: 05204309125463

STFR CALIBRATOR (UDI 05204309125463)

Manufactured by Medicon Hellas SA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STFR CALIBRATOR - Primary ID 05204309125463

Device Regulatory Overview

The STFR CALIBRATOR (Model/Catalog Number: 1478-0749) is a medical device manufactured by Medicon Hellas SA. This product is indexed under FDA Product Code / Category Classification W0102152206 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1478-0749
Product Code / EMDN
W0102152206
Device Name
STFR
Database Sync Date
2026-08-09 18:46:38

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 STFR CALIBRATOR?

The registered manufacturer of record for STFR CALIBRATOR is Medicon Hellas SA.

What is the Primary UDI-DI identifier for STFR CALIBRATOR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05204309125463.

What classification code is assigned to this device?

This device is registered under product classification code W0102152206.

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