GUDIDData
gudid Primary ID: 6987R

Assembly, Hand Pendant, ProAxis, Refurb (UDI 6987R)

Manufactured by MIZUHO ORTHOPEDIC SYSTEMS, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Assembly, Hand Pendant, ProAxis, Refurb - Primary ID 6987R

Device Regulatory Overview

The Assembly, Hand Pendant, ProAxis, Refurb (Model/Catalog Number: 6987R) is a medical device manufactured by MIZUHO ORTHOPEDIC SYSTEMS, INC.. This product is indexed under FDA Product Code / Category Classification JEA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
6987R
Product Code / EMDN
JEA
Device Name
Database Sync Date
2026-08-09 09:13:56

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Assembly, Hand Pendant, ProAxis, Refurb?

The registered manufacturer of record for Assembly, Hand Pendant, ProAxis, Refurb is MIZUHO ORTHOPEDIC SYSTEMS, INC..

What is the Primary UDI-DI identifier for Assembly, Hand Pendant, ProAxis, Refurb?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6987R.

What classification code is assigned to this device?

This device is registered under product classification code JEA.

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