gudid Primary ID: 5092

Bucket (UDI 5092)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Bucket (Model/Catalog Number: 5092) is a medical device manufactured by Andreas Hettich GmbH. This product is indexed under FDA Product Code / Category Classification KSO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 5092
Product Code / EMDN: KSO
Device Name: Centrifuge Bucket / Tube Holder A device intended to compensate for and enable the use of different size test tubes and bottles in a centrifuge rotor bucket or centrifuge tube holder. This is a reusable device.
Database Sync Date: 2026-08-09 09:26:15

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 Bucket?

The registered manufacturer of record for Bucket is Andreas Hettich GmbH.

What is the Primary UDI-DI identifier for Bucket?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5092.

What classification code is assigned to this device?

This device is registered under product classification code KSO.

Similar Classification Devices (KSO)

Other Devices by Andreas Hettich GmbH

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