Activator AC (UDI 9300)

Manufactured by VOCO GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Activator AC (Model/Catalog Number: 9300) 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: 9300
Product Code / EMDN: EJB
Device Name
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 Activator AC?

The registered manufacturer of record for Activator AC is VOCO GmbH.

What is the Primary UDI-DI identifier for Activator AC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9300.

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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