GUDIDData
eudamed_udi Primary ID: 08435440200208

CerTest Astrovirus (UDI 08435440200208)

Manufactured by CERTEST BIOTEC S.L.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CerTest Astrovirus - Primary ID 08435440200208

Device Regulatory Overview

The CerTest Astrovirus (Model/Catalog Number: AT820001V) is a medical device manufactured by CERTEST BIOTEC S.L.. This product is indexed under FDA Product Code / Category Classification W0105099099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AT820001V
Product Code / EMDN
W0105099099
Device Name
CerTest Astrovirus
Database Sync Date
2026-08-09 16:29:44

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 CerTest Astrovirus?

The registered manufacturer of record for CerTest Astrovirus is CERTEST BIOTEC S.L..

What is the Primary UDI-DI identifier for CerTest Astrovirus?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08435440200208.

What classification code is assigned to this device?

This device is registered under product classification code W0105099099.

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