gudid
Primary ID: 6713-1745
Paeon Anterior Cervical Plate System (UDI 6713-1745)
Manufactured by Aegis Spine, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Paeon Anterior Cervical Plate System - Primary ID 6713-1745
Device Regulatory Overview
The Paeon Anterior Cervical Plate System (Model/Catalog Number: 6713-1745) is a medical device manufactured by Aegis Spine, Inc.. This product is indexed under FDA Product Code / Category Classification KWQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6713-1745
- Product Code / EMDN
- KWQ
- Device Name
- Cervical Plate Contour Type 3 Level 45mm
- Database Sync Date
- 2026-08-09 09:12:08
Full Regulatory Attributes
🔒 Token Gated
{
"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 Paeon Anterior Cervical Plate System?
The registered manufacturer of record for Paeon Anterior Cervical Plate System is Aegis Spine, Inc..
What is the Primary UDI-DI identifier for Paeon Anterior Cervical Plate System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6713-1745.
What classification code is assigned to this device?
This device is registered under product classification code KWQ.
Similar Classification Devices (KWQ)
Other Devices by Aegis Spine, Inc.
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