MRI Patient Monitoring System Tesla M3 (UDI TeslaM3)
Manufactured by MIPM Mammendorfer Institut fr Physik und Medizin GmbH
Device Regulatory Overview
The MRI Patient Monitoring System Tesla M3 (Model/Catalog Number: TeslaM3) 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
- TeslaM3
- Product Code / EMDN
- MWI
- Device Name
- The MRI Patient Monitoring System Tesla M3 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
}
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 MRI Patient Monitoring System Tesla M3?
The registered manufacturer of record for MRI Patient Monitoring System Tesla M3 is MIPM Mammendorfer Institut fr Physik und Medizin GmbH.
What is the Primary UDI-DI identifier for MRI Patient Monitoring System Tesla M3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TeslaM3.
What classification code is assigned to this device?
This device is registered under product classification code MWI.
Similar Classification Devices (MWI)
Other Devices by MIPM Mammendorfer Institut fr Physik und Medizin GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint