gudid Primary ID: 176 030

n.a. (UDI 176 030)

Manufactured by Karl Storz GmbH & Co. KG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The n.a. (Model/Catalog Number: 176 030) is a medical device manufactured by Karl Storz GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification EKS within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 176 030
Product Code / EMDN: EKS
Device Name: LEMPERT Mastoid Curette. Size:000
Database Sync Date: 2026-08-09 09:07:45

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 n.a.?

The registered manufacturer of record for n.a. is Karl Storz GmbH & Co. KG.

What is the Primary UDI-DI identifier for n.a.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 176 030.

What classification code is assigned to this device?

This device is registered under product classification code EKS.

Similar Classification Devices (EKS)

Other Devices by Karl Storz GmbH & Co. KG

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