gudid Primary ID: 13920NKS

SILVER SCOPE (UDI 13920NKS)

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 SILVER SCOPE (Model/Catalog Number: 13920NKS) is a medical device manufactured by Karl Storz GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification FDF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 13920NKS
Product Code / EMDN: FDF
Device Name: Sigmoidoscope 11.2/3.4/800 NTSC
Database Sync Date: 2026-08-09 09:11:31

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 SILVER SCOPE?

The registered manufacturer of record for SILVER SCOPE is Karl Storz GmbH & Co. KG.

What is the Primary UDI-DI identifier for SILVER SCOPE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 13920NKS.

What classification code is assigned to this device?

This device is registered under product classification code FDF.

Similar Classification Devices (FDF)

Other Devices by Karl Storz GmbH & Co. KG

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