eudamed_udi
Primary ID: 10843471150068
Pro-Matrix Narrow (UDI 10843471150068)
Manufactured by Young Innovations Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pro-Matrix Narrow - Primary ID 10843471150068
Device Regulatory Overview
The Pro-Matrix Narrow (Model/Catalog Number: 19000) is a medical device manufactured by Young Innovations Inc. This product is indexed under FDA Product Code / Category Classification Q0199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 19000
- Product Code / EMDN
- Q0199
- Device Name
- Pro-Matrix Retainer Matrix
- Database Sync Date
- 2026-08-09 16:28:46
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 Pro-Matrix Narrow?
The registered manufacturer of record for Pro-Matrix Narrow is Young Innovations Inc.
What is the Primary UDI-DI identifier for Pro-Matrix Narrow?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10843471150068.
What classification code is assigned to this device?
This device is registered under product classification code Q0199.
Similar Classification Devices (Q0199)
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