GUDIDData
eudamed_udi Primary ID: 08435440205210

VIASURE Clostridium difficile toxins A+B Real Time PCR Detection Kit (UDI 08435440205210)

Manufactured by CERTEST BIOTEC S.L.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VIASURE Clostridium difficile toxins A+B Real Time PCR Detection Kit - Primary ID 08435440205210

Device Regulatory Overview

The VIASURE Clostridium difficile toxins A+B Real Time PCR Detection Kit (Model/Catalog Number: VS-CDA113H) is a medical device manufactured by CERTEST BIOTEC S.L.. This product is indexed under FDA Product Code / Category Classification W0105011804 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
VS-CDA113H
Product Code / EMDN
W0105011804
Device Name
VIASURE Clostridium difficile toxins A+B Real Time PCR Detection Kit
Database Sync Date
2026-08-09 18:52:23

Full Regulatory Attributes

đŸ”’ Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of VIASURE Clostridium difficile toxins A+B Real Time PCR Detection Kit?

The registered manufacturer of record for VIASURE Clostridium difficile toxins A+B Real Time PCR Detection Kit is CERTEST BIOTEC S.L..

What is the Primary UDI-DI identifier for VIASURE Clostridium difficile toxins A+B Real Time PCR Detection Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435440205210.

What classification code is assigned to this device?

This device is registered under product classification code W0105011804.

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