eudamed_udi
Primary ID: 08594199923452
BHI broth 5ml (UDI 08594199923452)
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 BHI broth 5ml - Primary ID 08594199923452
Device Regulatory Overview
The BHI broth 5ml (Model/Catalog Number: 98475-200) is a medical device manufactured by VIAMAR INTERNATIONAL, s.r.o.. This product is indexed under FDA Product Code / Category Classification W0104010206 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 98475-200
- Product Code / EMDN
- W0104010206
- Device Name
- Játrový bujón
- Database Sync Date
- 2026-08-09 16:48:34
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 BHI broth 5ml?
The registered manufacturer of record for BHI broth 5ml is VIAMAR INTERNATIONAL, s.r.o..
What is the Primary UDI-DI identifier for BHI broth 5ml?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594199923452.
What classification code is assigned to this device?
This device is registered under product classification code W0104010206.
Similar Classification Devices (W0104010206)
Other Devices by VIAMAR INTERNATIONAL, s.r.o.
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