GUDIDData
gudid Primary ID: 510-050-100

RZ Medizintechnik GmbH (UDI 510-050-100)

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 510-050-100

Device Regulatory Overview

The RZ Medizintechnik GmbH (Model/Catalog Number: 510-050-100) is a medical device manufactured by RZ-Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification GAC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
510-050-100
Product Code / EMDN
GAC
Device Name
Nail file, 10cm
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 510-050-100.

What classification code is assigned to this device?

This device is registered under product classification code GAC.

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