eudamed_udi
Primary ID: 06973596010149
Neo-Guard (UDI 06973596010149)
Manufactured by Conlett Technology Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neo-Guard - Primary ID 06973596010149
Device Regulatory Overview
The Neo-Guard (Model/Catalog Number: NG-000) is a medical device manufactured by Conlett Technology Inc. This product is indexed under FDA Product Code / Category Classification M0303010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NG-000
- Product Code / EMDN
- M0303010203
- Device Name
- Neo-Guard
- Database Sync Date
- 2026-08-09 17:04:40
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-Guard?
The registered manufacturer of record for Neo-Guard is Conlett Technology Inc.
What is the Primary UDI-DI identifier for Neo-Guard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973596010149.
What classification code is assigned to this device?
This device is registered under product classification code M0303010203.
Similar Classification Devices (M0303010203)
Other Devices by Conlett Technology Inc
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