eudamed_udi Primary ID: G520MD48060

Bone Graft Syringe (UDI G520MD48060)

Manufactured by Medspo

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Bone Graft Syringe (Model/Catalog Number: MD4806) is a medical device manufactured by Medspo. This product is indexed under FDA Product Code / Category Classification P01020101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MD4806
Product Code / EMDN: P01020101
Device Name: Bone Graft Syringe
Database Sync Date: 2026-08-09 16:46:53

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 Bone Graft Syringe?

The registered manufacturer of record for Bone Graft Syringe is Medspo.

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G520MD48060.

What classification code is assigned to this device?

This device is registered under product classification code P01020101.

Similar Classification Devices (P01020101)

Other Devices by Medspo

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