eudamed_udi
Primary ID: 08593540508799
Cievka endobronchiálna CE-600 (UDI 08593540508799)
Manufactured by GAMA GROUP a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cievka endobronchiálna CE-600 - Primary ID 08593540508799
Device Regulatory Overview
The Cievka endobronchiálna CE-600 (Model/Catalog Number: V606452-ND) 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-ND
- Product Code / EMDN
- R010499
- Device Name
- Cévka endobronchiální CE-600
- Database Sync Date
- 2026-08-09 17:49:33
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 Cievka endobronchiálna CE-600?
The registered manufacturer of record for Cievka endobronchiálna CE-600 is GAMA GROUP a.s..
What is the Primary UDI-DI identifier for Cievka endobronchiálna CE-600?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08593540508799.
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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