GUDIDData
eudamed_udi Primary ID: 05907514600311

AURYX 90 25-OH VD Reagent Kit (UDI 05907514600311)

Manufactured by PZ CORMAY Spółka Akcyjna

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AURYX 90 25-OH VD Reagent Kit - Primary ID 05907514600311

Device Regulatory Overview

The AURYX 90 25-OH VD Reagent Kit (Model/Catalog Number: I20-R0059) is a medical device manufactured by PZ CORMAY Spółka Akcyjna. This product is indexed under FDA Product Code / Category Classification W0102060309 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
I20-R0059
Product Code / EMDN
W0102060309
Device Name
AURYX 90 25-OH VD Reagent Kit
Database Sync Date
2026-08-09 17:15:30

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 AURYX 90 25-OH VD Reagent Kit?

The registered manufacturer of record for AURYX 90 25-OH VD Reagent Kit is PZ CORMAY Spółka Akcyjna.

What is the Primary UDI-DI identifier for AURYX 90 25-OH VD Reagent Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907514600311.

What classification code is assigned to this device?

This device is registered under product classification code W0102060309.

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