gudid Primary ID: 20325-223

ERBE (UDI 20325-223)

Manufactured by Erbe Elektromedizin GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ERBE (Model/Catalog Number: 20325-223) is a medical device manufactured by Erbe Elektromedizin GmbH. This product is indexed under FDA Product Code / Category Classification OCX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 20325-223
Product Code / EMDN: OCX
Device Name: Endoscopy Pump Tubing/ Cap Set for Fujinon Scopes
Database Sync Date: 2026-08-09 09:11:21

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 ERBE?

The registered manufacturer of record for ERBE is Erbe Elektromedizin GmbH.

What is the Primary UDI-DI identifier for ERBE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20325-223.

What classification code is assigned to this device?

This device is registered under product classification code OCX.

Similar Classification Devices (OCX)

Other Devices by Erbe Elektromedizin GmbH

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