eudamed_udi
Primary ID: 08594161958413
GeneProof Cytomegalovirus (CMV) PCR Kit (UDI 08594161958413)
Manufactured by GeneProof a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GeneProof Cytomegalovirus (CMV) PCR Kit - Primary ID 08594161958413
Device Regulatory Overview
The GeneProof Cytomegalovirus (CMV) PCR Kit (Model/Catalog Number: CMV/GP/100) is a medical device manufactured by GeneProof a.s.. This product is indexed under FDA Product Code / Category Classification W0105040205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CMV/GP/100
- Product Code / EMDN
- W0105040205
- Device Name
- GeneProof Cytomegalovirus (CMV) PCR Kit
- Database Sync Date
- 2026-08-09 17:10:09
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 GeneProof Cytomegalovirus (CMV) PCR Kit?
The registered manufacturer of record for GeneProof Cytomegalovirus (CMV) PCR Kit is GeneProof a.s..
What is the Primary UDI-DI identifier for GeneProof Cytomegalovirus (CMV) PCR Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08594161958413.
What classification code is assigned to this device?
This device is registered under product classification code W0105040205.
Similar Classification Devices (W0105040205)
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