gudid Primary ID: Dual-Spore

Spore Check System (UDI Dual-Spore)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Spore Check System (Model/Catalog Number: Dual-Spore) is a medical device manufactured by OSHA REVIEW INC. This product is indexed under FDA Product Code / Category Classification FRC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Dual-Spore
Product Code / EMDN: FRC
Device Name: Biological Indicator
Database Sync Date: 2026-08-09 09:00:34

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 Spore Check System?

The registered manufacturer of record for Spore Check System is OSHA REVIEW INC.

What is the Primary UDI-DI identifier for Spore Check System?

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

What classification code is assigned to this device?

This device is registered under product classification code FRC.

Similar Classification Devices (FRC)

Other Devices by OSHA REVIEW INC

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