gudid Primary ID: 4782-4

Bucket (UDI 4782-4)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Bucket (Model/Catalog Number: 4782-4) is a medical device manufactured by Andreas Hettich GmbH. This product is indexed under FDA Product Code / Category Classification JQC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 4782-4
Product Code / EMDN: JQC
Device Name: Centrifuge Bucket / Tube Holder (set of 4 matched units)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 09:26:14

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 4782-4.

What classification code is assigned to this device?

This device is registered under product classification code JQC.

Similar Classification Devices (JQC)

Other Devices by Andreas Hettich GmbH

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