eudamed_udi
Primary ID: 06973596010422
Neo-Oris 75ml (UDI 06973596010422)
Manufactured by Conlett Technology Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neo-Oris 75ml - Primary ID 06973596010422
Device Regulatory Overview
The Neo-Oris 75ml (Model/Catalog Number: NO075) is a medical device manufactured by Conlett Technology Inc. This product is indexed under FDA Product Code / Category Classification A06030301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NO075
- Product Code / EMDN
- A06030301
- Device Name
- Neo-Oris
- Database Sync Date
- 2026-08-09 17:05:58
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 Neo-Oris 75ml?
The registered manufacturer of record for Neo-Oris 75ml is Conlett Technology Inc.
What is the Primary UDI-DI identifier for Neo-Oris 75ml?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973596010422.
What classification code is assigned to this device?
This device is registered under product classification code A06030301.
Similar Classification Devices (A06030301)
Other Devices by Conlett Technology Inc
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