eudamed_udi
Primary ID: 03858892125946
BioSap HO, 10 L (UDI 03858892125946)
Manufactured by BioGnost Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BioSap HO, 10 L - Primary ID 03858892125946
Device Regulatory Overview
The BioSap HO, 10 L (Model/Catalog Number: DKKO-10L) is a medical device manufactured by BioGnost Ltd.. This product is indexed under FDA Product Code / Category Classification W0104010104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DKKO-10L
- Product Code / EMDN
- W0104010104
- Device Name
- Dodaci hranjivim podlogama
- Database Sync Date
- 2026-08-09 16:46:04
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 BioSap HO, 10 L?
The registered manufacturer of record for BioSap HO, 10 L is BioGnost Ltd..
What is the Primary UDI-DI identifier for BioSap HO, 10 L?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892125946.
What classification code is assigned to this device?
This device is registered under product classification code W0104010104.
Similar Classification Devices (W0104010104)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint