eudamed_udi
Primary ID: 08594199923384
PureChrom UTI (UDI 08594199923384)
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 PureChrom UTI - Primary ID 08594199923384
Device Regulatory Overview
The PureChrom UTI (Model/Catalog Number: 98464-20) is a medical device manufactured by VIAMAR INTERNATIONAL, s.r.o.. This product is indexed under FDA Product Code / Category Classification W0104010402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 98464-20
- Product Code / EMDN
- W0104010402
- Device Name
- PureChrom UTI
- Database Sync Date
- 2026-08-09 16:45:58
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 PureChrom UTI?
The registered manufacturer of record for PureChrom UTI is VIAMAR INTERNATIONAL, s.r.o..
What is the Primary UDI-DI identifier for PureChrom UTI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594199923384.
What classification code is assigned to this device?
This device is registered under product classification code W0104010402.
Similar Classification Devices (W0104010402)
Other Devices by VIAMAR INTERNATIONAL, s.r.o.
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