eudamed_udi
Primary ID: 08593540512994
Unspecified Brand (UDI 08593540512994)
Manufactured by GAMA GROUP a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08593540512994
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: V606301-01ND) 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
- V606301-01ND
- Product Code / EMDN
- A03020101
- Device Name
- GAMAPLUS 1,8 x 450 LLK
- Database Sync Date
- 2026-08-09 16:51:42
Full Regulatory Attributes
đź”’ Token Gated
{
"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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is GAMA GROUP a.s..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08593540512994.
What classification code is assigned to this device?
This device is registered under product classification code A03020101.
Similar Classification Devices (A03020101)
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