gudid
Primary ID: EKA-SEA
Orantech (UDI EKA-SEA)
Manufactured by Orantech Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Orantech - Primary ID EKA-SEA
Device Regulatory Overview
The Orantech (Model/Catalog Number: EKA-SEA) is a medical device manufactured by Orantech Inc.. This product is indexed under FDA Product Code / Category Classification DRX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EKA-SEA
- Product Code / EMDN
- DRX
- Device Name
- Suction Electrode Adapter Sets, 6pcs/Box
- Database Sync Date
- 2026-08-09 09:04:49
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 Orantech?
The registered manufacturer of record for Orantech is Orantech Inc..
What is the Primary UDI-DI identifier for Orantech?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EKA-SEA.
What classification code is assigned to this device?
This device is registered under product classification code DRX.
Similar Classification Devices (DRX)
Other Devices by Orantech Inc.
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