gudid
Primary ID: BFBA-0250
BiFORM Bioactive Moldable (UDI BFBA-0250)
Manufactured by COLLAGEN MATRIX, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BiFORM Bioactive Moldable - Primary ID BFBA-0250
Device Regulatory Overview
The BiFORM Bioactive Moldable (Model/Catalog Number: BFBA-0250) 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-0250
- 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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Get API Token Access ($49/mo)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-0250.
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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