GUDIDData
eudamed_udi Primary ID: 04260648815602

HeartSave myPAD 675A (UDI 04260648815602)

Manufactured by Metrax GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HeartSave myPAD 675A - Primary ID 04260648815602

Device Regulatory Overview

The HeartSave myPAD 675A (Model/Catalog Number: 98013) is a medical device manufactured by Metrax GmbH. This product is indexed under FDA Product Code / Category Classification Z12030503 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
98013
Product Code / EMDN
Z12030503
Device Name
myPAD
Database Sync Date
2026-08-09 16:45:49

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 HeartSave myPAD 675A?

The registered manufacturer of record for HeartSave myPAD 675A is Metrax GmbH.

What is the Primary UDI-DI identifier for HeartSave myPAD 675A?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260648815602.

What classification code is assigned to this device?

This device is registered under product classification code Z12030503.

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