gudid
Primary ID: 102435
PROFILE-V MEDTOXScan (UDI 102435)
Manufactured by MEDTOX DIAGNOSTICS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PROFILE-V MEDTOXScan - Primary ID 102435
Device Regulatory Overview
The PROFILE-V MEDTOXScan (Model/Catalog Number: 102435) 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
- 102435
- Product Code / EMDN
- DIF
- Device Name
- Positive toxicology urine control used to monitor and validate the performance of PROFILE-V MEDTOXScan drugs of abuse test devices.
- 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 PROFILE-V MEDTOXScan?
The registered manufacturer of record for PROFILE-V MEDTOXScan is MEDTOX DIAGNOSTICS, INC..
What is the Primary UDI-DI identifier for PROFILE-V MEDTOXScan?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 102435.
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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