eudamed_udi
Primary ID: 06973596010392
Neo-Teneo Rectangular (UDI 06973596010392)
Manufactured by Conlett Technology Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neo-Teneo Rectangular - Primary ID 06973596010392
Device Regulatory Overview
The Neo-Teneo Rectangular (Model/Catalog Number: NT-001) is a medical device manufactured by Conlett Technology Inc. This product is indexed under FDA Product Code / Category Classification V080302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NT-001
- Product Code / EMDN
- V080302
- Device Name
- NT-001
- Database Sync Date
- 2026-08-09 18:05:39
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 Neo-Teneo Rectangular?
The registered manufacturer of record for Neo-Teneo Rectangular is Conlett Technology Inc.
What is the Primary UDI-DI identifier for Neo-Teneo Rectangular?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973596010392.
What classification code is assigned to this device?
This device is registered under product classification code V080302.
Similar Classification Devices (V080302)
Other Devices by Conlett Technology Inc
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