eudamed_udi Primary ID: 08683347941438

RapidFor™ Strep A Rapid Test Kit (UDI 08683347941438)

Manufactured by Vitrosens Biotechnology Inc.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The RapidFor™ Strep A Rapid Test Kit (Model/Catalog Number: VMD36) is a medical device manufactured by Vitrosens Biotechnology Inc.. This product is indexed under FDA Product Code / Category Classification W0105090103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: VMD36
Product Code / EMDN: W0105090103
Device Name: RapidFor™ Strep A Rapid Test Kit
Database Sync Date: 2026-08-09 16:28:44

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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Frequently Asked Questions

Who is the primary manufacturer of RapidFor™ Strep A Rapid Test Kit?

The registered manufacturer of record for RapidFor™ Strep A Rapid Test Kit is Vitrosens Biotechnology Inc..

What is the Primary UDI-DI identifier for RapidFor™ Strep A Rapid Test Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683347941438.

What classification code is assigned to this device?

This device is registered under product classification code W0105090103.

Similar Classification Devices (W0105090103)

Other Devices by Vitrosens Biotechnology Inc.

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RapidFor­™ Strep A Rapid Test Kit (UDI 08683347941438)