gudid Primary ID: 570187-0

Suction bag, folded, 3000 ml (UDI 570187-0)

Manufactured by Serres Oy

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Suction bag, folded, 3000 ml (Model/Catalog Number: 570187-0) is a medical device manufactured by Serres Oy. This product is indexed under FDA Product Code / Category Classification KDQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 570187-0
Product Code / EMDN: KDQ
Device Name
Database Sync Date: 2026-08-09 09:24:56

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 Suction bag, folded, 3000 ml?

The registered manufacturer of record for Suction bag, folded, 3000 ml is Serres Oy.

What is the Primary UDI-DI identifier for Suction bag, folded, 3000 ml?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 570187-0.

What classification code is assigned to this device?

This device is registered under product classification code KDQ.

Similar Classification Devices (KDQ)

Other Devices by Serres Oy

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