Selenite broth 200 ml (UDI 08594199920321)
Manufactured by VIAMAR INTERNATIONAL, s.r.o.
Device Regulatory Overview
The Selenite broth 200 ml (Model/Catalog Number: 98035-1) is a medical device manufactured by VIAMAR INTERNATIONAL, s.r.o.. This product is indexed under FDA Product Code / Category Classification W0104010306 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 98035-1
- Product Code / EMDN
- W0104010306
- Device Name
- Selenitový bujón
- Database Sync Date
- 2026-08-09 16:30:02
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 Selenite broth 200 ml?
The registered manufacturer of record for Selenite broth 200 ml is VIAMAR INTERNATIONAL, s.r.o..
What is the Primary UDI-DI identifier for Selenite broth 200 ml?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594199920321.
What classification code is assigned to this device?
This device is registered under product classification code W0104010306.
Similar Classification Devices (W0104010306)
Other Devices by VIAMAR INTERNATIONAL, s.r.o.
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