GUDIDData
eudamed_udi Primary ID: 08055510562908

CYTO CUVETTE KIT 1 - 1 pozzetto, vetrino molato banda bianca (UDI 08055510562908)

Manufactured by Kaltek S.r.l.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CYTO CUVETTE KIT 1 - 1 pozzetto, vetrino molato banda bianca - Primary ID 08055510562908

Device Regulatory Overview

The CYTO CUVETTE KIT 1 - 1 pozzetto, vetrino molato banda bianca (Model/Catalog Number: 0671) is a medical device manufactured by Kaltek S.r.l.. This product is indexed under FDA Product Code / Category Classification W0503010203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
0671
Product Code / EMDN
W0503010203
Device Name
CUVETTE
Database Sync Date
2026-08-09 18:05:27

Full Regulatory Attributes

🔒 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 CYTO CUVETTE KIT 1 - 1 pozzetto, vetrino molato banda bianca?

The registered manufacturer of record for CYTO CUVETTE KIT 1 - 1 pozzetto, vetrino molato banda bianca is Kaltek S.r.l..

What is the Primary UDI-DI identifier for CYTO CUVETTE KIT 1 - 1 pozzetto, vetrino molato banda bianca?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055510562908.

What classification code is assigned to this device?

This device is registered under product classification code W0503010203.

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