gudid
Primary ID: 195 090 200
Urology syringe (UDI 195 090 200)
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 195 090 200
Device Regulatory Overview
The Urology syringe (Model/Catalog Number: 195 090 200) 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
- 195 090 200
- Product Code / EMDN
- FJL
- Device Name
- Database Sync Date
- 2026-08-09 09:11:48
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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Get API Token Access ($49/mo)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 195 090 200.
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
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JSON API Endpoint