GUDIDData
eudamed_udi Primary ID: 08606018770625

Chromogenic Candida Agar Plate (UDI 08606018770625)

Manufactured by DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Chromogenic Candida Agar Plate - Primary ID 08606018770625

Device Regulatory Overview

The Chromogenic Candida Agar Plate (Model/Catalog Number: PRM1297AV60) is a medical device manufactured by DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA. This product is indexed under FDA Product Code / Category Classification W0104010402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PRM1297AV60
Product Code / EMDN
W0104010402
Device Name
Chromogenic Candida Agar Plate
Database Sync Date
2026-08-09 16:46:23

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 Chromogenic Candida Agar Plate?

The registered manufacturer of record for Chromogenic Candida Agar Plate is DRUŠTVO ZA TRGOVINU I USLUGE PROMEDIA DOO KIKINDA.

What is the Primary UDI-DI identifier for Chromogenic Candida Agar Plate?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08606018770625.

What classification code is assigned to this device?

This device is registered under product classification code W0104010402.

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