GUDIDData
gudid Primary ID: 250-025-300

RZ Medizintechnik GmbH (UDI 250-025-300)

Manufactured by RZ-Medizintechnik GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RZ Medizintechnik GmbH - Primary ID 250-025-300

Device Regulatory Overview

The RZ Medizintechnik GmbH (Model/Catalog Number: 250-025-300) is a medical device manufactured by RZ-Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification EQH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
250-025-300
Product Code / EMDN
EQH
Device Name
Fibre Optic Light Guide Cable 2,5mm, 3000mm
Database Sync Date
2026-08-09 09:11:23

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 RZ Medizintechnik GmbH?

The registered manufacturer of record for RZ Medizintechnik GmbH is RZ-Medizintechnik GmbH.

What is the Primary UDI-DI identifier for RZ Medizintechnik GmbH?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 250-025-300.

What classification code is assigned to this device?

This device is registered under product classification code EQH.

Programmatic Export

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

JSON API Endpoint