Bismarck Brown Y boja u prahu, C.I. 21000, 25 g (UDI 03858888820626)
Manufactured by BioGnost Ltd.
Device Regulatory Overview
The Bismarck Brown Y boja u prahu, C.I. 21000, 25 g (Model/Catalog Number: BB-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
- BB-P-25
- Product Code / EMDN
- W01030707
- Device Name
- Boje u prahu
- Database Sync Date
- 2026-08-09 17:04:19
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 Bismarck Brown Y boja u prahu, C.I. 21000, 25 g?
The registered manufacturer of record for Bismarck Brown Y boja u prahu, C.I. 21000, 25 g is BioGnost Ltd..
What is the Primary UDI-DI identifier for Bismarck Brown Y boja u prahu, C.I. 21000, 25 g?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858888820626.
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