gudid Primary ID: 259-197-000

RZ Medizintechnik GmbH (UDI 259-197-000)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The RZ Medizintechnik GmbH (Model/Catalog Number: 259-197-000) is a medical device manufactured by RZ-Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification GAD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 259-197-000
Product Code / EMDN: GAD
Device Name: LT Lumbar Retraction Set
Database Sync Date: 2026-08-09 09:11:23

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 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 259-197-000.

What classification code is assigned to this device?

This device is registered under product classification code GAD.

Similar Classification Devices (GAD)

Other Devices by RZ-Medizintechnik GmbH

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