gudid Primary ID: 186 558 001BC001

Ureterorenoscope (UDI 186 558 001BC001)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Ureterorenoscope (Model/Catalog Number: 186 558 001BC001) is a medical device manufactured by SOPRO-COMEG GmbH. This product is indexed under FDA Product Code / Category Classification FJL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 186 558 001BC001
Product Code / EMDN: FJL
Device Name
Database Sync Date: 2026-08-09 09:11:49

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 Ureterorenoscope?

The registered manufacturer of record for Ureterorenoscope is SOPRO-COMEG GmbH.

What is the Primary UDI-DI identifier for Ureterorenoscope?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 186 558 001BC001.

What classification code is assigned to this device?

This device is registered under product classification code FJL.

Similar Classification Devices (FJL)

Other Devices by SOPRO-COMEG GmbH

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