GUDIDData
eudamed_udi Primary ID: 08594199922745

Helicobacter pylori agar (UDI 08594199922745)

Manufactured by VIAMAR INTERNATIONAL, s.r.o.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Helicobacter pylori agar - Primary ID 08594199922745

Device Regulatory Overview

The Helicobacter pylori agar (Model/Catalog Number: 98397-10) is a medical device manufactured by VIAMAR INTERNATIONAL, s.r.o.. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
98397-10
Product Code / EMDN
W0104010405
Device Name
Helicobacter pylori agar
Database Sync Date
2026-08-09 17:04:16

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 Helicobacter pylori agar?

The registered manufacturer of record for Helicobacter pylori agar is VIAMAR INTERNATIONAL, s.r.o..

What is the Primary UDI-DI identifier for Helicobacter pylori agar?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594199922745.

What classification code is assigned to this device?

This device is registered under product classification code W0104010405.

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