gudid Primary ID: NOVAPLUS PC KODIAK W/ IF MU LS

BREG (UDI NOVAPLUS PC KODIAK W/ IF MU LS)

Manufactured by BREG, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The BREG (Model/Catalog Number: NOVAPLUS PC KODIAK W/ IF MU LS) is a medical device manufactured by BREG, INC.. This product is indexed under FDA Product Code / Category Classification ILO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: NOVAPLUS PC KODIAK W/ IF MU LS
Product Code / EMDN: ILO
Device Name: 1 Ice Water Container, 1 6 VDC output, 120 VAC 60 Hz input transformer and 1 10245 I-Flo MU Long-Stem Pad
Database Sync Date: 2026-08-09 09:17:27

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 BREG?

The registered manufacturer of record for BREG is BREG, INC..

What is the Primary UDI-DI identifier for BREG?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NOVAPLUS PC KODIAK W/ IF MU LS.

What classification code is assigned to this device?

This device is registered under product classification code ILO.

Similar Classification Devices (ILO)

Other Devices by BREG, INC.

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