eudamed_udi
Primary ID: 03858892125410
Hematoksilin IHC, 1 L (UDI 03858892125410)
Manufactured by BioGnost Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hematoksilin IHC, 1 L - Primary ID 03858892125410
Device Regulatory Overview
The Hematoksilin IHC, 1 L (Model/Catalog Number: IHC-HEM-1L) is a medical device manufactured by BioGnost Ltd.. This product is indexed under FDA Product Code / Category Classification W01030799 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IHC-HEM-1L
- Product Code / EMDN
- W01030799
- Device Name
- Reagensi za procesiranje i pomoćni reagensi za histologiju/citologiju
- Database Sync Date
- 2026-08-09 16:28:50
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 Hematoksilin IHC, 1 L?
The registered manufacturer of record for Hematoksilin IHC, 1 L is BioGnost Ltd..
What is the Primary UDI-DI identifier for Hematoksilin IHC, 1 L?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03858892125410.
What classification code is assigned to this device?
This device is registered under product classification code W01030799.
Similar Classification Devices (W01030799)
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