gudid
Primary ID: 800-0710
Bilateral BMA Kit (UDI 800-0710)
Manufactured by Biomet Biologics, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bilateral BMA Kit - Primary ID 800-0710
Device Regulatory Overview
The Bilateral BMA Kit (Model/Catalog Number: 800-0710) is a medical device manufactured by Biomet Biologics, LLC. This product is indexed under FDA Product Code / Category Classification LWE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 800-0710
- Product Code / EMDN
- LWE
- Device Name
- Database Sync Date
- 2026-08-09 10:03:48
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 Bilateral BMA Kit?
The registered manufacturer of record for Bilateral BMA Kit is Biomet Biologics, LLC.
What is the Primary UDI-DI identifier for Bilateral BMA Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 800-0710.
What classification code is assigned to this device?
This device is registered under product classification code LWE.
Similar Classification Devices (LWE)
Other Devices by Biomet Biologics, LLC
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