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MRI Patient Moitor Tesla DUO

FDA UDI

Class II (US FDA UDI)

by MIPM Mammendorfer Institut für Physik und Medizin GmbH

Identity

Trade Name
MRI Patient Moitor Tesla DUO FDA UDI
Generic Name
MRI-patient physiologic monitoring system FDA UDI
Device Name
The MRI Patient Monitor TeslaDUO is intended for monitoring of vital signs during MRI examinations (MRI procedures) of patients. FDA UDI
Model / Reference
TeslaDUO FDA UDI
Description
The MRI Patient Monitor TeslaDUO is intended for monitoring of vital signs during MRI examinations (MRI procedures) of patients. FDA UDI

Identifiers

Catalog Number
1700001 FDA UDI
Primary DI / UDI-DI
EMIP17000010 FDA UDI
510(k) Number
K153739 FDA UDI
FDA Product Code
MWI FDA UDI
GMDN Term
MRI-patient physiologic monitoring system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: MRI-patient physiologic monitoring system

MRI Patient Moitor Tesla DUO by MIPM Mammendorfer Institut für Physik und Medizin GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as MRI-patient physiologic monitoring system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI abe516e2-d13f-49f5-b939-cecf7511623d 36 fields · synced May 30, 2026