eudamed_udi Primary ID: 06418685023209

Vacuum tube roll, silicone 5 m (UDI 06418685023209)

Manufactured by Serres Oy

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Vacuum tube roll, silicone 5 m (Model/Catalog Number: 57899-9) is a medical device manufactured by Serres Oy. This product is indexed under FDA Product Code / Category Classification A0680 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 57899-9
Product Code / EMDN: A0680
Device Name: Vacuum tube roll
Database Sync Date: 2026-08-09 16:28:52

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 Vacuum tube roll, silicone 5 m?

The registered manufacturer of record for Vacuum tube roll, silicone 5 m is Serres Oy.

What is the Primary UDI-DI identifier for Vacuum tube roll, silicone 5 m?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06418685023209.

What classification code is assigned to this device?

This device is registered under product classification code A0680.

Similar Classification Devices (A0680)

Other Devices by Serres Oy

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