gudid
Primary ID: M402 Clear
Original Posterior Matrix M Series (UDI M402 Clear)
Manufactured by Bioclear Matrix Systems
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Original Posterior Matrix M Series - Primary ID M402 Clear
Device Regulatory Overview
The Original Posterior Matrix M Series (Model/Catalog Number: M402 Clear) 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
- M402 Clear
- 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 Original Posterior Matrix M Series?
The registered manufacturer of record for Original Posterior Matrix M Series is Bioclear Matrix Systems.
What is the Primary UDI-DI identifier for Original Posterior Matrix M Series?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M402 Clear.
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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