gudid
Primary ID: 81-2054[US]
Bioplate (UDI 81-2054[US])
Manufactured by Bioplate, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bioplate - Primary ID 81-2054[US]
Device Regulatory Overview
The Bioplate (Model/Catalog Number: 81-2054[US]) is a medical device manufactured by Bioplate, Inc.. This product is indexed under FDA Product Code / Category Classification GXR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 81-2054[US]
- Product Code / EMDN
- GXR
- Device Name
- Flexible Burr Hole Cover - 1.5 mm - 6 hole - 18 mm
- Database Sync Date
- 2026-08-09 09:14:40
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 Bioplate?
The registered manufacturer of record for Bioplate is Bioplate, Inc..
What is the Primary UDI-DI identifier for Bioplate?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 81-2054[US].
What classification code is assigned to this device?
This device is registered under product classification code GXR.
Similar Classification Devices (GXR)
Other Devices by Bioplate, Inc.
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