eudamed_udi Primary ID: 08594199922394

Todd-Hewitt broth for GBS (UDI 08594199922394)

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 Todd-Hewitt broth for GBS (Model/Catalog Number: 98360-40) is a medical device manufactured by VIAMAR INTERNATIONAL, s.r.o.. This product is indexed under FDA Product Code / Category Classification W0104010206 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 98360-40
Product Code / EMDN: W0104010206
Device Name: Todd-Hewitt bujón pro GBS
Database Sync Date: 2026-08-09 16:58:08

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 Todd-Hewitt broth for GBS?

The registered manufacturer of record for Todd-Hewitt broth for GBS is VIAMAR INTERNATIONAL, s.r.o..

What is the Primary UDI-DI identifier for Todd-Hewitt broth for GBS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594199922394.

What classification code is assigned to this device?

This device is registered under product classification code W0104010206.

Similar Classification Devices (W0104010206)

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

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