eudamed_udi
Primary ID: 08593540354129
Petriho miska Ø 90 mm AP dvousektorová (UDI 08593540354129)
Manufactured by GAMA GROUP a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Petriho miska Ø 90 mm AP dvousektorová - Primary ID 08593540354129
Device Regulatory Overview
The Petriho miska Ø 90 mm AP dvousektorová (Model/Catalog Number: V204421) is a medical device manufactured by GAMA GROUP a.s.. This product is indexed under FDA Product Code / Category Classification W0503030101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V204421
- Product Code / EMDN
- W0503030101
- Device Name
- Petriho miska Ø 90 mm AP
- Database Sync Date
- 2026-08-09 16:45:40
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 Petriho miska Ø 90 mm AP dvousektorová?
The registered manufacturer of record for Petriho miska Ø 90 mm AP dvousektorová is GAMA GROUP a.s..
What is the Primary UDI-DI identifier for Petriho miska Ø 90 mm AP dvousektorová?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08593540354129.
What classification code is assigned to this device?
This device is registered under product classification code W0503030101.
Similar Classification Devices (W0503030101)
Other Devices by GAMA GROUP a.s.
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