gudid Primary ID: 110035371

BIOMET BONE CEMENT R (UDI 110035371)

Manufactured by BIOMET

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

Scannable UDI-DI Representation

Device Regulatory Overview

The BIOMET BONE CEMENT R (Model/Catalog Number: 110035371) is a medical device manufactured by BIOMET. This product is indexed under FDA Product Code / Category Classification LOD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 110035371
Product Code / EMDN: LOD
Device Name
Database Sync Date: 2026-08-09 09:55:05

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 BIOMET BONE CEMENT R?

The registered manufacturer of record for BIOMET BONE CEMENT R is BIOMET.

What is the Primary UDI-DI identifier for BIOMET BONE CEMENT R?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 110035371.

What classification code is assigned to this device?

This device is registered under product classification code LOD.

Similar Classification Devices (LOD)

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