gudid Primary ID: EVRPLUS-G

Everion+ System (UDI EVRPLUS-G)

Manufactured by BIOFOURMIS SINGAPORE PTE. LTD.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Everion+ System (Model/Catalog Number: EVRPLUS-G) is a medical device manufactured by BIOFOURMIS SINGAPORE PTE. LTD.. This product is indexed under FDA Product Code / Category Classification MWI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: EVRPLUS-G
Product Code / EMDN: MWI
Device Name: Everion+ System
Database Sync Date: 2026-08-09 09:15:12

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 Everion+ System?

The registered manufacturer of record for Everion+ System is BIOFOURMIS SINGAPORE PTE. LTD..

What is the Primary UDI-DI identifier for Everion+ System?

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

What classification code is assigned to this device?

This device is registered under product classification code MWI.

Similar Classification Devices (MWI)

Other Devices by BIOFOURMIS SINGAPORE PTE. LTD.

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