AURYX 90 TESTO Reagent Kit (UDI 05907514601424)
Manufactured by PZ CORMAY Spółka Akcyjna
Device Regulatory Overview
The AURYX 90 TESTO Reagent Kit (Model/Catalog Number: I20-R0088) is a medical device manufactured by PZ CORMAY Spółka Akcyjna. This product is indexed under FDA Product Code / Category Classification W0102050110 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- I20-R0088
- Product Code / EMDN
- W0102050110
- Device Name
- AURYX 90 TESTO Reagent Kit
- Database Sync Date
- 2026-08-09 17:02:13
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 AURYX 90 TESTO Reagent Kit?
The registered manufacturer of record for AURYX 90 TESTO Reagent Kit is PZ CORMAY Spółka Akcyjna.
What is the Primary UDI-DI identifier for AURYX 90 TESTO Reagent Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907514601424.
What classification code is assigned to this device?
This device is registered under product classification code W0102050110.
Similar Classification Devices (W0102050110)
Other Devices by PZ CORMAY Spółka Akcyjna
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint