gudid Primary ID: MS32610

S/W SUB VF9.1.1 INFINITY EXPLORER (UDI MS32610)

Manufactured by DRAEGER MEDICAL SYSTEMS, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The S/W SUB VF9.1.1 INFINITY EXPLORER (Model/Catalog Number: MS32610) is a medical device manufactured by DRAEGER MEDICAL SYSTEMS, INC.. This product is indexed under FDA Product Code / Category Classification MSX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MS32610
Product Code / EMDN: MSX
Device Name
Database Sync Date: 2026-08-09 09:11:27

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 S/W SUB VF9.1.1 INFINITY EXPLORER?

The registered manufacturer of record for S/W SUB VF9.1.1 INFINITY EXPLORER is DRAEGER MEDICAL SYSTEMS, INC..

What is the Primary UDI-DI identifier for S/W SUB VF9.1.1 INFINITY EXPLORER?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MS32610.

What classification code is assigned to this device?

This device is registered under product classification code MSX.

Similar Classification Devices (MSX)

Other Devices by DRAEGER MEDICAL SYSTEMS, INC.

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