eudamed_udi
Primary ID: 03858892125144
BioSap CS, 10 mL (UDI 03858892125144)
Manufactured by BioGnost Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BioSap CS, 10 mL - Primary ID 03858892125144
Device Regulatory Overview
The BioSap CS, 10 mL (Model/Catalog Number: KOE-010) 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
- KOE-010
- Product Code / EMDN
- W0104010104
- Device Name
- Dodaci hranjivim podlogama
- Database Sync Date
- 2026-08-09 17:09:42
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 CS, 10 mL?
The registered manufacturer of record for BioSap CS, 10 mL is BioGnost Ltd..
What is the Primary UDI-DI identifier for BioSap CS, 10 mL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892125144.
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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