eudamed_udi
Primary ID: 05904708000742
Fungisel Agar (UDI 05904708000742)
Manufactured by GRASO Zenon Sobiecki
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fungisel Agar - Primary ID 05904708000742
Device Regulatory Overview
The Fungisel Agar (Model/Catalog Number: 1240PD90) is a medical device manufactured by GRASO Zenon Sobiecki. This product is indexed under FDA Product Code / Category Classification W0104030201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1240PD90
- Product Code / EMDN
- W0104030201
- Device Name
- Fungisel Agar
- Database Sync Date
- 2026-08-09 16:50:10
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 Fungisel Agar?
The registered manufacturer of record for Fungisel Agar is GRASO Zenon Sobiecki.
What is the Primary UDI-DI identifier for Fungisel Agar?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904708000742.
What classification code is assigned to this device?
This device is registered under product classification code W0104030201.
Similar Classification Devices (W0104030201)
Other Devices by GRASO Zenon Sobiecki
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