gudid
Primary ID: 186 405 001
Ureterorenoscope (UDI 186 405 001)
Manufactured by SOPRO-COMEG GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ureterorenoscope - Primary ID 186 405 001
Device Regulatory Overview
The Ureterorenoscope (Model/Catalog Number: 186 405 001) 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
- 186 405 001
- 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
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)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 186 405 001.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint