eudamed_udi Primary ID: 00840277130280

Intramedullary Nail Remover Set (UDI 00840277130280)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Intramedullary Nail Remover Set (Model/Catalog Number: 2027-20) 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...

🔒 Compromised Lot & Serial Numbers Locked

Verify if facility inventory is affected by this recall.

Unlock Lot Data ($49)

Technical Specifications

Model Number: 2027-20
Product Code / EMDN: L0921
Device Name: Extractor
Database Sync Date: 2026-08-09 16:28:53

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Intramedullary Nail Remover Set?

The registered manufacturer of record for Intramedullary Nail Remover Set is Innomed, Inc..

What is the Primary UDI-DI identifier for Intramedullary Nail Remover Set?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840277130280.

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.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint