eudamed_udi Primary ID: 08593540513854

GAMAPLUS® 3,0 x 150 LCH M (UDI 08593540513854)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The GAMAPLUS® 3,0 x 150 LCH M (Model/Catalog Number: V606372-M) is a medical device manufactured by GAMA GROUP a.s.. This product is indexed under FDA Product Code / Category Classification A03020101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: V606372-M
Product Code / EMDN: A03020101
Device Name: GAMAPLUS
Database Sync Date: 2026-08-09 16:28:47

Full Regulatory Attributes

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{
    "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 GAMAPLUS® 3,0 x 150 LCH M?

The registered manufacturer of record for GAMAPLUS® 3,0 x 150 LCH M is GAMA GROUP a.s..

What is the Primary UDI-DI identifier for GAMAPLUS® 3,0 x 150 LCH M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08593540513854.

What classification code is assigned to this device?

This device is registered under product classification code A03020101.

Similar Classification Devices (A03020101)

Other Devices by GAMA GROUP a.s.

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