GUDIDData
gudid Primary ID: MS18785

Inf Explorer Monitor (Software) (UDI MS18785)

Manufactured by DRAEGER MEDICAL SYSTEMS, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Inf Explorer Monitor (Software) - Primary ID MS18785

Device Regulatory Overview

The Inf Explorer Monitor (Software) (Model/Catalog Number: MS18785) 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
MS18785
Product Code / EMDN
MSX
Device Name
Database Sync Date
2026-08-09 09:11:27

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Inf Explorer Monitor (Software)?

The registered manufacturer of record for Inf Explorer Monitor (Software) is DRAEGER MEDICAL SYSTEMS, INC..

What is the Primary UDI-DI identifier for Inf Explorer Monitor (Software)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MS18785.

What classification code is assigned to this device?

This device is registered under product classification code MSX.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint