eudamed_udi
Primary ID: 08594199920215
XLD agar (UDI 08594199920215)
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 XLD agar - Primary ID 08594199920215
Device Regulatory Overview
The XLD agar (Model/Catalog Number: 98024-20) is a medical device manufactured by VIAMAR INTERNATIONAL, s.r.o.. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 98024-20
- Product Code / EMDN
- W0104010405
- Device Name
- XLD agar
- Database Sync Date
- 2026-08-09 16:49:38
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 XLD agar?
The registered manufacturer of record for XLD agar is VIAMAR INTERNATIONAL, s.r.o..
What is the Primary UDI-DI identifier for XLD agar?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594199920215.
What classification code is assigned to this device?
This device is registered under product classification code W0104010405.
Similar Classification Devices (W0104010405)
Other Devices by VIAMAR INTERNATIONAL, s.r.o.
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