gudid
Primary ID: DBM050
InterGro DBM Plus (UDI DBM050)
Manufactured by Biomet Orthopedics, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for InterGro DBM Plus - Primary ID DBM050
Device Regulatory Overview
The InterGro DBM Plus (Model/Catalog Number: DBM050) is a medical device manufactured by Biomet Orthopedics, LLC. This product is indexed under FDA Product Code / Category Classification GXP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DBM050
- Product Code / EMDN
- GXP
- Device Name
- Porous Hydroxyapatite Bone Graft Substitute
- Database Sync Date
- 2026-08-09 09:43:05
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 InterGro DBM Plus?
The registered manufacturer of record for InterGro DBM Plus is Biomet Orthopedics, LLC.
What is the Primary UDI-DI identifier for InterGro DBM Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DBM050.
What classification code is assigned to this device?
This device is registered under product classification code GXP.
Similar Classification Devices (GXP)
Other Devices by Biomet Orthopedics, LLC
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