eudamed_udi
Primary ID: 08593540507808
Infúzna súprava IS-103 – bal. 4x50 ks (UDI 08593540507808)
Manufactured by GAMA GROUP a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Infúzna súprava IS-103 – bal. 4x50 ks - Primary ID 08593540507808
Device Regulatory Overview
The Infúzna súprava IS-103 – bal. 4x50 ks (Model/Catalog Number: V606103-01ND) is a medical device manufactured by GAMA GROUP a.s.. This product is indexed under FDA Product Code / Category Classification A03040199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V606103-01ND
- Product Code / EMDN
- A03040199
- Device Name
- Infúzní souprava pro gravitační infúze
- Database Sync Date
- 2026-08-09 16:46:10
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 Infúzna súprava IS-103 – bal. 4x50 ks?
The registered manufacturer of record for Infúzna súprava IS-103 – bal. 4x50 ks is GAMA GROUP a.s..
What is the Primary UDI-DI identifier for Infúzna súprava IS-103 – bal. 4x50 ks?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08593540507808.
What classification code is assigned to this device?
This device is registered under product classification code A03040199.
Similar Classification Devices (A03040199)
Other Devices by GAMA GROUP a.s.
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