GUDIDData
gudid Primary ID: M1230849

EVair (UDI M1230849)

Manufactured by IMT Analytics AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EVair - Primary ID M1230849

Device Regulatory Overview

The EVair (Model/Catalog Number: M1230849) is a medical device manufactured by IMT Analytics AG. This product is indexed under FDA Product Code / Category Classification BTI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
M1230849
Product Code / EMDN
BTI
Device Name
The medical air compressor is intended for use as an integrated, optional accessory to provide a dry, filtered, breathable compressed air supply to GE Datex-Ohmeda Engstrm Carestation and Engstrm Pro ventilators.
Database Sync Date
2026-08-09 09:16:07

Full Regulatory Attributes

🔒 Token Gated
{
    "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 EVair?

The registered manufacturer of record for EVair is IMT Analytics AG.

What is the Primary UDI-DI identifier for EVair?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M1230849.

What classification code is assigned to this device?

This device is registered under product classification code BTI.

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