GUDIDData
eudamed_udi Primary ID: 08594199921151

Carbolfuchsin 1000ml (Gram) (UDI 08594199921151)

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 Carbolfuchsin 1000ml (Gram) - Primary ID 08594199921151

Device Regulatory Overview

The Carbolfuchsin 1000ml (Gram) (Model/Catalog Number: 98231-2) is a medical device manufactured by VIAMAR INTERNATIONAL, s.r.o.. This product is indexed under FDA Product Code / Category Classification W0104010804 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
98231-2
Product Code / EMDN
W0104010804
Device Name
Karbolfuchsin 1000ml (Gram)
Database Sync Date
2026-08-09 17:02:36

Full Regulatory Attributes

đź”’ 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 Carbolfuchsin 1000ml (Gram)?

The registered manufacturer of record for Carbolfuchsin 1000ml (Gram) is VIAMAR INTERNATIONAL, s.r.o..

What is the Primary UDI-DI identifier for Carbolfuchsin 1000ml (Gram)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594199921151.

What classification code is assigned to this device?

This device is registered under product classification code W0104010804.

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