GUDIDData
eudamed_udi Primary ID: 08593540508959

Cievka odsávacia s CO, 1 BO, 2,67mm (Ch 8) x 400 mm (UDI 08593540508959)

Manufactured by GAMA GROUP a.s.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cievka odsávacia s CO, 1 BO, 2,67mm (Ch 8) x 400 mm - Primary ID 08593540508959

Device Regulatory Overview

The Cievka odsávacia s CO, 1 BO, 2,67mm (Ch 8) x 400 mm (Model/Catalog Number: V646739-ND) is a medical device manufactured by GAMA GROUP a.s.. This product is indexed under FDA Product Code / Category Classification R010499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
V646739-ND
Product Code / EMDN
R010499
Device Name
Cévka odsávací s CO, 1 BO, 2,67mm (Ch 8) x 400 mm
Database Sync Date
2026-08-09 18:57:10

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 Cievka odsávacia s CO, 1 BO, 2,67mm (Ch 8) x 400 mm?

The registered manufacturer of record for Cievka odsávacia s CO, 1 BO, 2,67mm (Ch 8) x 400 mm is GAMA GROUP a.s..

What is the Primary UDI-DI identifier for Cievka odsávacia s CO, 1 BO, 2,67mm (Ch 8) x 400 mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08593540508959.

What classification code is assigned to this device?

This device is registered under product classification code R010499.

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