eudamed_udi Primary ID: 14544753010334

Pre-gelled bag 2000 ml (UDI 14544753010334)

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 2000 ml (Model/Catalog Number: 57567-0JP) 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: 57567-0JP
Product Code / EMDN: A060301
Device Name: Suction bags
Database Sync Date: 2026-08-09 16:51:23

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Pre-gelled bag 2000 ml?

The registered manufacturer of record for Pre-gelled bag 2000 ml is Serres Oy.

What is the Primary UDI-DI identifier for Pre-gelled bag 2000 ml?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 14544753010334.

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

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint