eudamed_udi
Primary ID: 08593540513984
Cévka endobronchiální CE-600 M (UDI 08593540513984)
Manufactured by GAMA GROUP a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cévka endobronchiální CE-600 M - Primary ID 08593540513984
Device Regulatory Overview
The Cévka endobronchiální CE-600 M (Model/Catalog Number: V606452-M) 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
- V606452-M
- Product Code / EMDN
- R010499
- Device Name
- Cévka odsávací (endobronchiální)
- Database Sync Date
- 2026-08-09 18:26:30
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 Cévka endobronchiální CE-600 M?
The registered manufacturer of record for Cévka endobronchiální CE-600 M is GAMA GROUP a.s..
What is the Primary UDI-DI identifier for Cévka endobronchiální CE-600 M?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08593540513984.
What classification code is assigned to this device?
This device is registered under product classification code R010499.
Similar Classification Devices (R010499)
Other Devices by GAMA GROUP a.s.
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