GUDIDData
eudamed_udi Primary ID: 08684595032541

DrugFor™ UR-144 Rapid Test Kit (Urine) (UDI 08684595032541)

Manufactured by Vitrosens Biotechnology Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DrugFor™ UR-144 Rapid Test Kit (Urine) - Primary ID 08684595032541

Device Regulatory Overview

The DrugFor™ UR-144 Rapid Test Kit (Urine) (Model/Catalog Number: VDDOA33) is a medical device manufactured by Vitrosens Biotechnology Inc.. This product is indexed under FDA Product Code / Category Classification W0102160505 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
VDDOA33
Product Code / EMDN
W0102160505
Device Name
UR-144 Rapid Test Kit (Urine)
Database Sync Date
2026-08-09 16:29:50

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of DrugFor™ UR-144 Rapid Test Kit (Urine)?

The registered manufacturer of record for DrugFor™ UR-144 Rapid Test Kit (Urine) is Vitrosens Biotechnology Inc..

What is the Primary UDI-DI identifier for DrugFor™ UR-144 Rapid Test Kit (Urine)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08684595032541.

What classification code is assigned to this device?

This device is registered under product classification code W0102160505.

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