gudid Primary ID: 20325-323

ERBE (UDI 20325-323)

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: 20325-323) 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: 20325-323
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

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

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 20325-323.

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

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint