GUDIDData
eudamed_udi Primary ID: 05907514600953

AURYX 90 Insulin Reagent Kit (UDI 05907514600953)

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 Insulin Reagent Kit - Primary ID 05907514600953

Device Regulatory Overview

The AURYX 90 Insulin Reagent Kit (Model/Catalog Number: I20-R0073) is a medical device manufactured by PZ CORMAY Spółka Akcyjna. This product is indexed under FDA Product Code / Category Classification W0102060103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
I20-R0073
Product Code / EMDN
W0102060103
Device Name
AURYX 90 Insulin Reagent Kit
Database Sync Date
2026-08-09 18:12:43

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 Insulin Reagent Kit?

The registered manufacturer of record for AURYX 90 Insulin Reagent Kit is PZ CORMAY Spółka Akcyjna.

What is the Primary UDI-DI identifier for AURYX 90 Insulin Reagent Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907514600953.

What classification code is assigned to this device?

This device is registered under product classification code W0102060103.

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