gudid
Primary ID: MFG-0101 1.0
ClearCorrect System (UDI MFG-0101 1.0)
Manufactured by Clearcorrect Operating, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ClearCorrect System - Primary ID MFG-0101 1.0
Device Regulatory Overview
The ClearCorrect System (Model/Catalog Number: MFG-0101 1.0) is a medical device manufactured by Clearcorrect Operating, LLC. This product is indexed under FDA Product Code / Category Classification NXC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MFG-0101 1.0
- Product Code / EMDN
- NXC
- Device Name
- Engager template device accessory for use with the ClearCorrect System.
- Database Sync Date
- 2026-08-09 09:03:36
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 ClearCorrect System?
The registered manufacturer of record for ClearCorrect System is Clearcorrect Operating, LLC.
What is the Primary UDI-DI identifier for ClearCorrect System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MFG-0101 1.0.
What classification code is assigned to this device?
This device is registered under product classification code NXC.
Similar Classification Devices (NXC)
Other Devices by Clearcorrect Operating, LLC
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