eudamed_udi Primary ID: 03597610547911

IGOSAFE ASPIRATION (UDI 03597610547911)

Manufactured by D.M.D.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The IGOSAFE ASPIRATION (Model/Catalog Number: 2923484Y5) is a medical device manufactured by D.M.D.. This product is indexed under FDA Product Code / Category Classification D99 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2923484Y5
Product Code / EMDN: D99
Device Name: IGOSAFE ASPIRATION 1X5L
Database Sync Date: 2026-08-09 18:04:59

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 IGOSAFE ASPIRATION?

The registered manufacturer of record for IGOSAFE ASPIRATION is D.M.D..

What is the Primary UDI-DI identifier for IGOSAFE ASPIRATION?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03597610547911.

What classification code is assigned to this device?

This device is registered under product classification code D99.

Similar Classification Devices (D99)

Other Devices by D.M.D.

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