eudamed_udi
Primary ID: 03858888820657
Leishman Stain boja u prahu, 25 g (UDI 03858888820657)
Manufactured by BioGnost Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Leishman Stain boja u prahu, 25 g - Primary ID 03858888820657
Device Regulatory Overview
The Leishman Stain boja u prahu, 25 g (Model/Catalog Number: LS-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
- LS-P-25
- Product Code / EMDN
- W01030707
- Device Name
- Boje u prahu
- Database Sync Date
- 2026-08-09 18:21:49
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 Leishman Stain boja u prahu, 25 g?
The registered manufacturer of record for Leishman Stain boja u prahu, 25 g is BioGnost Ltd..
What is the Primary UDI-DI identifier for Leishman Stain boja u prahu, 25 g?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858888820657.
What classification code is assigned to this device?
This device is registered under product classification code W01030707.
Similar Classification Devices (W01030707)
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