eudamed_udi
Primary ID: 06971819180556
Cure Trio (UDI 06971819180556)
Manufactured by Netop Industrial Company Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cure Trio - Primary ID 06971819180556
Device Regulatory Overview
The Cure Trio (Model/Catalog Number: MC-310S) is a medical device manufactured by Netop Industrial Company Limited. This product is indexed under FDA Product Code / Category Classification Z12062801 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MC-310S
- Product Code / EMDN
- Z12062801
- Device Name
- Cure Trio
- Database Sync Date
- 2026-08-09 17:14:31
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 Cure Trio?
The registered manufacturer of record for Cure Trio is Netop Industrial Company Limited.
What is the Primary UDI-DI identifier for Cure Trio?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971819180556.
What classification code is assigned to this device?
This device is registered under product classification code Z12062801.
Similar Classification Devices (Z12062801)
Other Devices by Netop Industrial Company Limited
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