eudamed_udi
Primary ID: 05997345782881
ETALON Teszt (UDI 05997345782881)
Manufactured by 77 Elektronika Műszeripari Kft
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ETALON Teszt - Primary ID 05997345782881
Device Regulatory Overview
The ETALON Teszt (Model/Catalog Number: ETN-9902) is a medical device manufactured by 77 Elektronika Műszeripari Kft. This product is indexed under FDA Product Code / Category Classification W0101060101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ETN-9902
- Product Code / EMDN
- W0101060101
- Device Name
- ETALON Teszt
- Database Sync Date
- 2026-08-09 16:28:48
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 ETALON Teszt?
The registered manufacturer of record for ETALON Teszt is 77 Elektronika Műszeripari Kft.
What is the Primary UDI-DI identifier for ETALON Teszt?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05997345782881.
What classification code is assigned to this device?
This device is registered under product classification code W0101060101.
Similar Classification Devices (W0101060101)
Other Devices by 77 Elektronika Műszeripari Kft
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