GUDIDData
eudamed_udi Primary ID: 03858892121634

Sirius Red boja u prahu, C.I. 35780, 25 g (UDI 03858892121634)

Manufactured by BioGnost Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sirius Red boja u prahu, C.I. 35780, 25 g - Primary ID 03858892121634

Device Regulatory Overview

The Sirius Red boja u prahu, C.I. 35780, 25 g (Model/Catalog Number: SR-P-25) is a medical device manufactured by BioGnost Ltd.. This product is indexed under FDA Product Code / Category Classification W01030707 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SR-P-25
Product Code / EMDN
W01030707
Device Name
Boje u prahu
Database Sync Date
2026-08-09 16:58:39

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Sirius Red boja u prahu, C.I. 35780, 25 g?

The registered manufacturer of record for Sirius Red boja u prahu, C.I. 35780, 25 g is BioGnost Ltd..

What is the Primary UDI-DI identifier for Sirius Red boja u prahu, C.I. 35780, 25 g?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892121634.

What classification code is assigned to this device?

This device is registered under product classification code W01030707.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint