gudid Primary ID: BFBA-0500

BiFORM Bioactive Moldable (UDI BFBA-0500)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The BiFORM Bioactive Moldable (Model/Catalog Number: BFBA-0500) is a medical device manufactured by COLLAGEN MATRIX, INC.. This product is indexed under FDA Product Code / Category Classification MQV within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: BFBA-0500
Product Code / EMDN: MQV
Device Name: Moldable Bone Graft Matrix
Database Sync Date: 2026-08-09 09:37:52

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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Frequently Asked Questions

Who is the primary manufacturer of BiFORM Bioactive Moldable?

The registered manufacturer of record for BiFORM Bioactive Moldable is COLLAGEN MATRIX, INC..

What is the Primary UDI-DI identifier for BiFORM Bioactive Moldable?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BFBA-0500.

What classification code is assigned to this device?

This device is registered under product classification code MQV.

Similar Classification Devices (MQV)

Other Devices by COLLAGEN MATRIX, INC.

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