eudamed_udi Primary ID: 00840277112668

Mueller Style Flat Blade Osteotome (UDI 00840277112668)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Mueller Style Flat Blade Osteotome (Model/Catalog Number: 6865-01) is a medical device manufactured by Innomed, Inc.. This product is indexed under FDA Product Code / Category Classification L090401 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1753-2024 View Full Alert →

INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup...

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Technical Specifications

Model Number: 6865-01
Product Code / EMDN: L090401
Device Name: Osteotome
Database Sync Date: 2026-08-09 16:29:30

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 Mueller Style Flat Blade Osteotome?

The registered manufacturer of record for Mueller Style Flat Blade Osteotome is Innomed, Inc..

What is the Primary UDI-DI identifier for Mueller Style Flat Blade Osteotome?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840277112668.

What classification code is assigned to this device?

This device is registered under product classification code L090401.

Similar Classification Devices (L090401)

Other Devices by Innomed, Inc.

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