GUDIDData
eudamed_udi Primary ID: 08593540514295

Cévka rektální s CO 6,67 mm (Ch 20) x 400 mm M (UDI 08593540514295)

Manufactured by GAMA GROUP a.s.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cévka rektální s CO 6,67 mm (Ch 20) x 400 mm M - Primary ID 08593540514295

Device Regulatory Overview

The Cévka rektální s CO 6,67 mm (Ch 20) x 400 mm M (Model/Catalog Number: V646688-M) is a medical device manufactured by GAMA GROUP a.s.. This product is indexed under FDA Product Code / Category Classification G020301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
V646688-M
Product Code / EMDN
G020301
Device Name
Cévka rektální
Database Sync Date
2026-08-09 16:58:36

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 Cévka rektální s CO 6,67 mm (Ch 20) x 400 mm M?

The registered manufacturer of record for Cévka rektální s CO 6,67 mm (Ch 20) x 400 mm M is GAMA GROUP a.s..

What is the Primary UDI-DI identifier for Cévka rektální s CO 6,67 mm (Ch 20) x 400 mm M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08593540514295.

What classification code is assigned to this device?

This device is registered under product classification code G020301.

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