gudid
Primary ID: 102520
MEDTOX (UDI 102520)
Manufactured by MEDTOX DIAGNOSTICS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEDTOX - Primary ID 102520
Device Regulatory Overview
The MEDTOX (Model/Catalog Number: 102520) is a medical device manufactured by MEDTOX DIAGNOSTICS, INC.. This product is indexed under FDA Product Code / Category Classification DIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 102520
- Product Code / EMDN
- DIF
- Device Name
- Positive toxicology urine control used to monitor and validate the performance of Labcorp Fentanyl (nFEN) tests.
- Database Sync Date
- 2026-08-09 09:04:21
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 MEDTOX?
The registered manufacturer of record for MEDTOX is MEDTOX DIAGNOSTICS, INC..
What is the Primary UDI-DI identifier for MEDTOX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 102520.
What classification code is assigned to this device?
This device is registered under product classification code DIF.
Similar Classification Devices (DIF)
Other Devices by MEDTOX DIAGNOSTICS, INC.
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