GUDIDData
gudid Primary ID: TeslaDUO

MRI Patient Monitor TeslaDUO (UDI TeslaDUO)

Manufactured by MIPM Mammendorfer Institut fr Physik und Medizin GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MRI Patient Monitor TeslaDUO - Primary ID TeslaDUO

Device Regulatory Overview

The MRI Patient Monitor TeslaDUO (Model/Catalog Number: TeslaDUO) is a medical device manufactured by MIPM Mammendorfer Institut fr Physik und Medizin GmbH. This product is indexed under FDA Product Code / Category Classification MWI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TeslaDUO
Product Code / EMDN
MWI
Device Name
The MRI Patient Monitor TeslaDUO is intended for monitoring of vital signs during MRI examinations (MRI procedures) of patients.
Database Sync Date
2026-08-09 09:17:36

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 MRI Patient Monitor TeslaDUO?

The registered manufacturer of record for MRI Patient Monitor TeslaDUO is MIPM Mammendorfer Institut fr Physik und Medizin GmbH.

What is the Primary UDI-DI identifier for MRI Patient Monitor TeslaDUO?

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

What classification code is assigned to this device?

This device is registered under product classification code MWI.

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