GUDIDData
gudid Primary ID: 6895-71

Adante FlexLation Spar, Right (UDI 6895-71)

Manufactured by MIZUHO ORTHOPEDIC SYSTEMS, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Adante FlexLation Spar, Right - Primary ID 6895-71

Device Regulatory Overview

The Adante FlexLation Spar, Right (Model/Catalog Number: 6895-71) 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
6895-71
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 Adante FlexLation Spar, Right?

The registered manufacturer of record for Adante FlexLation Spar, Right is MIZUHO ORTHOPEDIC SYSTEMS, INC..

What is the Primary UDI-DI identifier for Adante FlexLation Spar, Right?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6895-71.

What classification code is assigned to this device?

This device is registered under product classification code JEA.

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