eudamed_udi
Primary ID: 08593540507532
Prevodová súprava PS (UDI 08593540507532)
Manufactured by GAMA GROUP a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Prevodová súprava PS - Primary ID 08593540507532
Device Regulatory Overview
The Prevodová súprava PS (Model/Catalog Number: V606386-03ND) is a medical device manufactured by GAMA GROUP a.s.. This product is indexed under FDA Product Code / Category Classification A03040202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V606386-03ND
- Product Code / EMDN
- A03040202
- Device Name
- Převodová souprava PS
- Database Sync Date
- 2026-08-09 16:29:45
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Prevodová súprava PS?
The registered manufacturer of record for Prevodová súprava PS is GAMA GROUP a.s..
What is the Primary UDI-DI identifier for Prevodová súprava PS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08593540507532.
What classification code is assigned to this device?
This device is registered under product classification code A03040202.
Similar Classification Devices (A03040202)
Other Devices by GAMA GROUP a.s.
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