N/A (UDI 31012764)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The N/A (Model/Catalog Number: 31012764) is a medical device manufactured by MEDTRONIC XOMED, INC.. This product is indexed under FDA Product Code / Category Classification EQJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 31012764
Product Code / EMDN: EQJ
Device Name: BUR 31012764 2.7MM 64MM L ACORN CARBIDE
Database Sync Date: 2026-08-09 09:17:18

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 N/A?

The registered manufacturer of record for N/A is MEDTRONIC XOMED, INC..

What is the Primary UDI-DI identifier for N/A?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 31012764.

What classification code is assigned to this device?

This device is registered under product classification code EQJ.

Similar Classification Devices (EQJ)

Other Devices by MEDTRONIC XOMED, INC.

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