eudamed_udi
Primary ID: 05060294771210
geko (UDI 05060294771210)
Manufactured by Firstkind Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for geko - Primary ID 05060294771210
Device Regulatory Overview
The geko (Model/Catalog Number: T3FE02) is a medical device manufactured by Firstkind Limited. This product is indexed under FDA Product Code / Category Classification N0199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- T3FE02
- Product Code / EMDN
- N0199
- Device Name
- Neuromuscular Electro-stimulation Device
- Database Sync Date
- 2026-08-09 16:28:58
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 geko?
The registered manufacturer of record for geko is Firstkind Limited.
What is the Primary UDI-DI identifier for geko?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060294771210.
What classification code is assigned to this device?
This device is registered under product classification code N0199.
Similar Classification Devices (N0199)
Other Devices by Firstkind Limited
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