eudamed_udi
Primary ID: 04260648815756
DefiSign myPAD DS (UDI 04260648815756)
Manufactured by Metrax GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DefiSign myPAD DS - Primary ID 04260648815756
Device Regulatory Overview
The DefiSign myPAD DS (Model/Catalog Number: 98028) is a medical device manufactured by Metrax GmbH. This product is indexed under FDA Product Code / Category Classification Z12030501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 98028
- Product Code / EMDN
- Z12030501
- Device Name
- myPAD
- Database Sync Date
- 2026-08-09 16:51:34
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of DefiSign myPAD DS?
The registered manufacturer of record for DefiSign myPAD DS is Metrax GmbH.
What is the Primary UDI-DI identifier for DefiSign myPAD DS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260648815756.
What classification code is assigned to this device?
This device is registered under product classification code Z12030501.
Similar Classification Devices (Z12030501)
Other Devices by Metrax GmbH
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