eudamed_udi Primary ID: 08594199920574

Blood agar (Columbia) / Endo agar (UDI 08594199920574)

Manufactured by VIAMAR INTERNATIONAL, s.r.o.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Blood agar (Columbia) / Endo agar (Model/Catalog Number: 98076-48) is a medical device manufactured by VIAMAR INTERNATIONAL, s.r.o.. This product is indexed under FDA Product Code / Category Classification W0104010407 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 98076-48
Product Code / EMDN: W0104010407
Device Name: Krevní agar / Endo agar
Database Sync Date: 2026-08-09 17:28:36

Full Regulatory Attributes

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{
    "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 Blood agar (Columbia) / Endo agar?

The registered manufacturer of record for Blood agar (Columbia) / Endo agar is VIAMAR INTERNATIONAL, s.r.o..

What is the Primary UDI-DI identifier for Blood agar (Columbia) / Endo agar?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594199920574.

What classification code is assigned to this device?

This device is registered under product classification code W0104010407.

Similar Classification Devices (W0104010407)

Other Devices by VIAMAR INTERNATIONAL, s.r.o.

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