eudamed_udi
Primary ID: 08594199920260
Sabouraud agar (UDI 08594199920260)
Manufactured by VIAMAR INTERNATIONAL, s.r.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sabouraud agar - Primary ID 08594199920260
Device Regulatory Overview
The Sabouraud agar (Model/Catalog Number: 98029-20) is a medical device manufactured by VIAMAR INTERNATIONAL, s.r.o.. This product is indexed under FDA Product Code / Category Classification W0104030201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 98029-20
- Product Code / EMDN
- W0104030201
- Device Name
- Sabouraud agar
- Database Sync Date
- 2026-08-09 17:55:45
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 Sabouraud agar?
The registered manufacturer of record for Sabouraud agar is VIAMAR INTERNATIONAL, s.r.o..
What is the Primary UDI-DI identifier for Sabouraud agar?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594199920260.
What classification code is assigned to this device?
This device is registered under product classification code W0104030201.
Similar Classification Devices (W0104030201)
Other Devices by VIAMAR INTERNATIONAL, s.r.o.
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