eudamed_udi Primary ID: 00840277112897

Cobra Retractor with Hand Rest (UDI 00840277112897)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Cobra Retractor with Hand Rest (Model/Catalog Number: 7130) 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: 7130
Product Code / EMDN: L0915
Device Name: Retractor
Database Sync Date: 2026-08-09 16:29:11

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 Cobra Retractor with Hand Rest?

The registered manufacturer of record for Cobra Retractor with Hand Rest is Innomed, Inc..

What is the Primary UDI-DI identifier for Cobra Retractor with Hand Rest?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840277112897.

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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