gudid Primary ID: 570587-0

Pre-gelled bag, folded, 3000 ml (UDI 570587-0)

Manufactured by Serres Oy

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Pre-gelled bag, folded, 3000 ml (Model/Catalog Number: 570587-0) 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: 570587-0
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 Pre-gelled bag, folded, 3000 ml?

The registered manufacturer of record for Pre-gelled bag, folded, 3000 ml is Serres Oy.

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 570587-0.

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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