GUDIDData
eudamed_udi Primary ID: E0HM36TCT090161

Bone Management (UDI E0HM36TCT090161)

Manufactured by Hager & Meisinger GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bone Management - Primary ID E0HM36TCT090161

Device Regulatory Overview

The Bone Management (Model/Catalog Number: 36TCT09016) is a medical device manufactured by Hager & Meisinger GmbH. This product is indexed under FDA Product Code / Category Classification P09120699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
36TCT09016
Product Code / EMDN
P09120699
Device Name
Products for bone fixation
Database Sync Date
2026-08-09 16:45:46

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Bone Management?

The registered manufacturer of record for Bone Management is Hager & Meisinger GmbH.

What is the Primary UDI-DI identifier for Bone Management?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is E0HM36TCT090161.

What classification code is assigned to this device?

This device is registered under product classification code P09120699.

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