eudamed_udi
Primary ID: 03858890001051
Orcein boja u prahu, C.I. (ed.1) 1242, 5 g (UDI 03858890001051)
Manufactured by BioGnost Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Orcein boja u prahu, C.I. (ed.1) 1242, 5 g - Primary ID 03858890001051
Device Regulatory Overview
The Orcein boja u prahu, C.I. (ed.1) 1242, 5 g (Model/Catalog Number: ORC-P-5) 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
- ORC-P-5
- Product Code / EMDN
- W01030707
- Device Name
- Boje u prahu
- Database Sync Date
- 2026-08-09 16:29:15
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 Orcein boja u prahu, C.I. (ed.1) 1242, 5 g?
The registered manufacturer of record for Orcein boja u prahu, C.I. (ed.1) 1242, 5 g is BioGnost Ltd..
What is the Primary UDI-DI identifier for Orcein boja u prahu, C.I. (ed.1) 1242, 5 g?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858890001051.
What classification code is assigned to this device?
This device is registered under product classification code W01030707.
Similar Classification Devices (W01030707)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint