eudamed_udi
Primary ID: 04260526920220
OkuEl Electrode Package (UDI 04260526920220)
Manufactured by Okuvision GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OkuEl Electrode Package - Primary ID 04260526920220
Device Regulatory Overview
The OkuEl Electrode Package (Model/Catalog Number: OK100310) is a medical device manufactured by Okuvision GmbH. This product is indexed under FDA Product Code / Category Classification Z12100385 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OK100310
- Product Code / EMDN
- Z12100385
- Device Name
- OkuEl Electrode Package
- Database Sync Date
- 2026-08-09 16:50:53
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 OkuEl Electrode Package?
The registered manufacturer of record for OkuEl Electrode Package is Okuvision GmbH.
What is the Primary UDI-DI identifier for OkuEl Electrode Package?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260526920220.
What classification code is assigned to this device?
This device is registered under product classification code Z12100385.
Similar Classification Devices (Z12100385)
Other Devices by Okuvision GmbH
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