eudamed_udi Primary ID: 06418685054012

Dual filter suction bag (UDI 06418685054012)

Manufactured by Serres Oy

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Dual filter suction bag (Model/Catalog Number: 57187-5) is a medical device manufactured by Serres Oy. This product is indexed under FDA Product Code / Category Classification A060301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 57187-5
Product Code / EMDN: A060301
Device Name: Suction bags
Database Sync Date: 2026-08-09 16:46:24

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 Dual filter suction bag?

The registered manufacturer of record for Dual filter suction bag is Serres Oy.

What is the Primary UDI-DI identifier for Dual filter suction bag?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06418685054012.

What classification code is assigned to this device?

This device is registered under product classification code A060301.

Similar Classification Devices (A060301)

Other Devices by Serres Oy

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