gudid
Primary ID: URS-11-50
TECO DIAGNOSTICS (UDI URS-11-50)
Manufactured by TECO DIAGNOSTICS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TECO DIAGNOSTICS - Primary ID URS-11-50
Device Regulatory Overview
The TECO DIAGNOSTICS (Model/Catalog Number: URS-11-50) is a medical device manufactured by TECO DIAGNOSTICS. This product is indexed under FDA Product Code / Category Classification LJX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- URS-11-50
- Product Code / EMDN
- LJX
- Device Name
- URS-11-50 TECO FINISHED KIT
- Database Sync Date
- 2026-08-09 10:01:14
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 TECO DIAGNOSTICS?
The registered manufacturer of record for TECO DIAGNOSTICS is TECO DIAGNOSTICS.
What is the Primary UDI-DI identifier for TECO DIAGNOSTICS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is URS-11-50.
What classification code is assigned to this device?
This device is registered under product classification code LJX.
Similar Classification Devices (LJX)
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