eudamed_udi Primary ID: 00840277114747

Fracture Pick Screw Removal (UDI 00840277114747)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Fracture Pick Screw Removal (Model/Catalog Number: S0129) is a medical device manufactured by Innomed, Inc.. This product is indexed under FDA Product Code / Category Classification L0921 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: S0129
Product Code / EMDN: L0921
Device Name: Extractor
Database Sync Date: 2026-08-09 16:28:52

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 Fracture Pick Screw Removal?

The registered manufacturer of record for Fracture Pick Screw Removal is Innomed, Inc..

What is the Primary UDI-DI identifier for Fracture Pick Screw Removal?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840277114747.

What classification code is assigned to this device?

This device is registered under product classification code L0921.

Similar Classification Devices (L0921)

Other Devices by Innomed, Inc.

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