gudid Primary ID: AS-322

PRAS BRU BBE/PEA Convenience Pack (UDI AS-322)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The PRAS BRU BBE/PEA Convenience Pack (Model/Catalog Number: AS-322) is a medical device manufactured by ANAEROBE SYSTEMS. This product is indexed under FDA Product Code / Category Classification KZI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AS-322
Product Code / EMDN: KZI
Device Name: AS-322 BRU and BBE/PEA Convenience Pack - Includes 1 Brucella Blood Agar (BRU) and 1 Bacteroides Bile Esculin Agar (BBE)/Phenylethyl Alcohol Blood Agar (PEA) Biplate. Pre-reduced anaerobically sterilized (PRAS). 100 x 15 mm agar plate. BRU is opaque burgundy red. BBE is transparent yellow/green. PEA is opaque red. 2 plates per pack.
Database Sync Date: 2026-08-09 09:10:00

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 PRAS BRU BBE/PEA Convenience Pack?

The registered manufacturer of record for PRAS BRU BBE/PEA Convenience Pack is ANAEROBE SYSTEMS.

What is the Primary UDI-DI identifier for PRAS BRU BBE/PEA Convenience Pack?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AS-322.

What classification code is assigned to this device?

This device is registered under product classification code KZI.

Similar Classification Devices (KZI)

Other Devices by ANAEROBE SYSTEMS

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