gudid
Primary ID: 1004930
Omega Connector Titanium (UDI 1004930)
Manufactured by Heinz Kurz GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Omega Connector Titanium - Primary ID 1004930
Device Regulatory Overview
The Omega Connector Titanium (Model/Catalog Number: 1004930) is a medical device manufactured by Heinz Kurz GmbH. This product is indexed under FDA Product Code / Category Classification ETA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1004930
- Product Code / EMDN
- ETA
- Device Name
- Ossicular Prosthesis, total
- Database Sync Date
- 2026-08-09 09:08:31
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 Omega Connector Titanium?
The registered manufacturer of record for Omega Connector Titanium is Heinz Kurz GmbH.
What is the Primary UDI-DI identifier for Omega Connector Titanium?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1004930.
What classification code is assigned to this device?
This device is registered under product classification code ETA.
Similar Classification Devices (ETA)
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