GUDIDData
gudid Primary ID: 195 091 000

Urology syringe (UDI 195 091 000)

Manufactured by SOPRO-COMEG GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Urology syringe - Primary ID 195 091 000

Device Regulatory Overview

The Urology syringe (Model/Catalog Number: 195 091 000) 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
195 091 000
Product Code / EMDN
FJL
Device Name
Database Sync Date
2026-08-09 09:11:48

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Urology syringe?

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

What is the Primary UDI-DI identifier for Urology syringe?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 195 091 000.

What classification code is assigned to this device?

This device is registered under product classification code FJL.

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