Dispenser (UDI 9302)

Manufactured by VOCO GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Dispenser (Model/Catalog Number: 9302) is a medical device manufactured by VOCO GmbH. This product is indexed under FDA Product Code / Category Classification EJB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 9302
Product Code / EMDN: EJB
Device Name: Dispenser Caps
Database Sync Date: 2026-08-09 09:07:36

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 Dispenser?

The registered manufacturer of record for Dispenser is VOCO GmbH.

What is the Primary UDI-DI identifier for Dispenser?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9302.

What classification code is assigned to this device?

This device is registered under product classification code EJB.

Similar Classification Devices (EJB)

Other Devices by VOCO GmbH

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