eudamed_udi Primary ID: 00840277108012

Stanton Forward Rake Retractor Deep (UDI 00840277108012)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Stanton Forward Rake Retractor Deep (Model/Catalog Number: 4512-02) is a medical device manufactured by Innomed, Inc.. This product is indexed under FDA Product Code / Category Classification L0915 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: 4512-02
Product Code / EMDN: L0915
Device Name: Retractor
Database Sync Date: 2026-08-09 16:30:32

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 Stanton Forward Rake Retractor Deep?

The registered manufacturer of record for Stanton Forward Rake Retractor Deep is Innomed, Inc..

What is the Primary UDI-DI identifier for Stanton Forward Rake Retractor Deep?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840277108012.

What classification code is assigned to this device?

This device is registered under product classification code L0915.

Similar Classification Devices (L0915)

Other Devices by Innomed, Inc.

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