GUDIDData
eudamed_udi Primary ID: 03858890004793

Fosfomolibdenska kiselina, 5%-tna otopina, 100 mL (UDI 03858890004793)

Manufactured by BioGnost Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fosfomolibdenska kiselina, 5%-tna otopina, 100 mL - Primary ID 03858890004793

Device Regulatory Overview

The Fosfomolibdenska kiselina, 5%-tna otopina, 100 mL (Model/Catalog Number: FMK5-OT-100) is a medical device manufactured by BioGnost Ltd.. This product is indexed under FDA Product Code / Category Classification W01030708 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FMK5-OT-100
Product Code / EMDN
W01030708
Device Name
Reagensi za bojenje
Database Sync Date
2026-08-09 16:28:46

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 Fosfomolibdenska kiselina, 5%-tna otopina, 100 mL?

The registered manufacturer of record for Fosfomolibdenska kiselina, 5%-tna otopina, 100 mL is BioGnost Ltd..

What is the Primary UDI-DI identifier for Fosfomolibdenska kiselina, 5%-tna otopina, 100 mL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858890004793.

What classification code is assigned to this device?

This device is registered under product classification code W01030708.

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