eudamed_udi Primary ID: G520MD2502D0

Tofflemire (UDI G520MD2502D0)

Manufactured by Medspo

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Tofflemire (Model/Catalog Number: MD2502D) is a medical device manufactured by Medspo. This product is indexed under FDA Product Code / Category Classification Q010399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MD2502D
Product Code / EMDN: Q010399
Device Name: Tofflemire
Database Sync Date: 2026-08-09 16:49:25

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 Tofflemire?

The registered manufacturer of record for Tofflemire is Medspo.

What is the Primary UDI-DI identifier for Tofflemire?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G520MD2502D0.

What classification code is assigned to this device?

This device is registered under product classification code Q010399.

Similar Classification Devices (Q010399)

Other Devices by Medspo

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