eudamed_udi
Primary ID: 03859891237999
Azure C boja u prahu, C.I. 52002, 25 g (UDI 03859891237999)
Manufactured by BioGnost Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Azure C boja u prahu, C.I. 52002, 25 g - Primary ID 03859891237999
Device Regulatory Overview
The Azure C boja u prahu, C.I. 52002, 25 g (Model/Catalog Number: AC-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
- AC-P-25
- Product Code / EMDN
- W01030707
- Device Name
- Boje u prahu
- Database Sync Date
- 2026-08-09 17:29:00
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 Azure C boja u prahu, C.I. 52002, 25 g?
The registered manufacturer of record for Azure C boja u prahu, C.I. 52002, 25 g is BioGnost Ltd..
What is the Primary UDI-DI identifier for Azure C boja u prahu, C.I. 52002, 25 g?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03859891237999.
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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