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Wireless Pulse Oximetry Sensor for TeslaDUO

FDA UDI

Class II (US FDA UDI)

by MIPM Mammendorfer Institut für Physik und Medizin GmbH

Identity

Trade Name
Wireless Pulse Oximetry Sensor for TeslaDUO FDA UDI
Generic Name
Patient monitoring system module, pulse oximetry FDA UDI
Model / Reference
Wireless Pulse Oximetry Sensor for TeslaDUO FDA UDI

Identifiers

Catalog Number
5010101 FDA UDI
Primary DI / UDI-DI
04255629200553 FDA UDI
510(k) Number
K153739 FDA UDI
FDA Product Code
MWI FDA UDI
GMDN Term
Patient monitoring system module, pulse oximetry 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: Patient monitoring system module, pulse oximetry

Wireless Pulse Oximetry Sensor for TeslaDUO by MIPM Mammendorfer Institut für Physik und Medizin GmbH — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Patient monitoring system module, pulse oximetry.

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 cbb21902-f00d-4a9e-b9f9-2e33b1f55505 35 fields · synced May 30, 2026