gudid
Primary ID: A101 HD
HD Anterior Matrix A Series (UDI A101 HD)
Manufactured by Bioclear Matrix Systems
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HD Anterior Matrix A Series - Primary ID A101 HD
Device Regulatory Overview
The HD Anterior Matrix A Series (Model/Catalog Number: A101 HD) is a medical device manufactured by Bioclear Matrix Systems. This product is indexed under FDA Product Code / Category Classification JEP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A101 HD
- Product Code / EMDN
- JEP
- Device Name
- Clear matrix used in dental restorations.
- Database Sync Date
- 2026-08-09 09:01:11
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 HD Anterior Matrix A Series?
The registered manufacturer of record for HD Anterior Matrix A Series is Bioclear Matrix Systems.
What is the Primary UDI-DI identifier for HD Anterior Matrix A Series?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A101 HD.
What classification code is assigned to this device?
This device is registered under product classification code JEP.
Similar Classification Devices (JEP)
Other Devices by Bioclear Matrix Systems
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