GUDIDData
eudamed_udi Primary ID: 04260648816272

BJÖRN myPAD BSD (UDI 04260648816272)

Manufactured by Metrax GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BJÖRN myPAD BSD - Primary ID 04260648816272

Device Regulatory Overview

The BJÖRN myPAD BSD (Model/Catalog Number: 98063) 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
98063
Product Code / EMDN
Z12030501
Device Name
myPAD
Database Sync Date
2026-08-09 16:48:32

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of BJÖRN myPAD BSD?

The registered manufacturer of record for BJÖRN myPAD BSD is Metrax GmbH.

What is the Primary UDI-DI identifier for BJÖRN myPAD BSD?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260648816272.

What classification code is assigned to this device?

This device is registered under product classification code Z12030501.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint