gudid Primary ID: 7510600

INFUSE Bone Graft (UDI 7510600)

Manufactured by MEDTRONIC SOFAMOR DANEK, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The INFUSE Bone Graft (Model/Catalog Number: 7510600) is a medical device manufactured by MEDTRONIC SOFAMOR DANEK, INC.. This product is indexed under FDA Product Code / Category Classification NPZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 7510600
Product Code / EMDN: NPZ
Device Name: BONE GRAFT KIT 7510600 INFUSE LARGE
Database Sync Date: 2026-08-09 09:17:19

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 INFUSE Bone Graft?

The registered manufacturer of record for INFUSE Bone Graft is MEDTRONIC SOFAMOR DANEK, INC..

What is the Primary UDI-DI identifier for INFUSE Bone Graft?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 7510600.

What classification code is assigned to this device?

This device is registered under product classification code NPZ.

Similar Classification Devices (NPZ)

Other Devices by MEDTRONIC SOFAMOR DANEK, INC.

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