eudamed_udi Primary ID: 00840277131829

Lee Buttress Pin Guide Set (UDI 00840277131829)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Lee Buttress Pin Guide Set (Model/Catalog Number: 3024-00) is a medical device manufactured by Innomed, Inc.. This product is indexed under FDA Product Code / Category Classification L0922 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: 3024-00
Product Code / EMDN: L0922
Device Name: Guide
Database Sync Date: 2026-08-09 16:28:56

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 Lee Buttress Pin Guide Set?

The registered manufacturer of record for Lee Buttress Pin Guide Set is Innomed, Inc..

What is the Primary UDI-DI identifier for Lee Buttress Pin Guide Set?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840277131829.

What classification code is assigned to this device?

This device is registered under product classification code L0922.

Similar Classification Devices (L0922)

Other Devices by Innomed, Inc.

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