eudamed_udi
Primary ID: 27350060320103
MRX PT Quick (UDI 27350060320103)
Manufactured by Nordic Biomarker AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MRX PT Quick - Primary ID 27350060320103
Device Regulatory Overview
The MRX PT Quick (Model/Catalog Number: K5024) is a medical device manufactured by Nordic Biomarker AB. This product is indexed under FDA Product Code / Category Classification W0103020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K5024
- Product Code / EMDN
- W0103020101
- Device Name
- PT Quick
- Database Sync Date
- 2026-08-09 16:29:37
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 MRX PT Quick?
The registered manufacturer of record for MRX PT Quick is Nordic Biomarker AB.
What is the Primary UDI-DI identifier for MRX PT Quick?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 27350060320103.
What classification code is assigned to this device?
This device is registered under product classification code W0103020101.
Similar Classification Devices (W0103020101)
Other Devices by Nordic Biomarker AB
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint