RapidFor™ Opiate (OPI) Rapid Test Kit (Urine) (UDI 08683548251428)
Manufactured by Vitrosens Biotechnology Inc.
Device Regulatory Overview
The RapidFor™ Opiate (OPI) Rapid Test Kit (Urine) (Model/Catalog Number: VDOA23) is a medical device manufactured by Vitrosens Biotechnology Inc.. This product is indexed under FDA Product Code / Category Classification W0102160508 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VDOA23
- Product Code / EMDN
- W0102160508
- Device Name
- Opiate (OPI) Rapid Test Kit (Urine)
- Database Sync Date
- 2026-08-09 16:30:20
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 RapidFor™ Opiate (OPI) Rapid Test Kit (Urine)?
The registered manufacturer of record for RapidFor™ Opiate (OPI) Rapid Test Kit (Urine) is Vitrosens Biotechnology Inc..
What is the Primary UDI-DI identifier for RapidFor™ Opiate (OPI) Rapid Test Kit (Urine)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683548251428.
What classification code is assigned to this device?
This device is registered under product classification code W0102160508.
Similar Classification Devices (W0102160508)
Other Devices by Vitrosens Biotechnology Inc.
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