eudamed_udi Primary ID: 00840277133557

RR2056-10 Osteotome (UDI 00840277133557)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The RR2056-10 Osteotome (Model/Catalog Number: 2056-10) is a medical device manufactured by Innomed, Inc.. This product is indexed under FDA Product Code / Category Classification L090401 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: 2056-10
Product Code / EMDN: L090401
Device Name: Osteotome
Database Sync Date: 2026-08-09 16:29:02

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 RR2056-10 Osteotome?

The registered manufacturer of record for RR2056-10 Osteotome is Innomed, Inc..

What is the Primary UDI-DI identifier for RR2056-10 Osteotome?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840277133557.

What classification code is assigned to this device?

This device is registered under product classification code L090401.

Similar Classification Devices (L090401)

Other Devices by Innomed, Inc.

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