gudid Primary ID: 400-01-295

DJO SURGICAL (UDI 400-01-295)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DJO SURGICAL (Model/Catalog Number: 400-01-295) is a medical device manufactured by Encore Medical, L.P.. This product is indexed under FDA Product Code / Category Classification MRA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 400-01-295
Product Code / EMDN: MRA
Device Name: Ceramic Head -4.0 - Size 32
Database Sync Date: 2026-08-09 09:19:32

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 DJO SURGICAL?

The registered manufacturer of record for DJO SURGICAL is Encore Medical, L.P..

What is the Primary UDI-DI identifier for DJO SURGICAL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 400-01-295.

What classification code is assigned to this device?

This device is registered under product classification code MRA.

Similar Classification Devices (MRA)

Other Devices by Encore Medical, L.P.

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