eudamed_udi
Primary ID: 03858892124932
BioSap SO, 50 mL (UDI 03858892124932)
Manufactured by BioGnost Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BioSap SO, 50 mL - Primary ID 03858892124932
Device Regulatory Overview
The BioSap SO, 50 mL (Model/Catalog Number: DOKO-050) 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
- DOKO-050
- Product Code / EMDN
- W0104010104
- Device Name
- Dodaci hranjivim podlogama
- Database Sync Date
- 2026-08-09 17:24:19
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BioSap SO, 50 mL?
The registered manufacturer of record for BioSap SO, 50 mL is BioGnost Ltd..
What is the Primary UDI-DI identifier for BioSap SO, 50 mL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892124932.
What classification code is assigned to this device?
This device is registered under product classification code W0104010104.
Similar Classification Devices (W0104010104)
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