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MyView™ Presence Tag

FDA UDI

Class II (US FDA UDI)

by Masimo Corporation

Identity

Trade Name
MyView™ Presence Tag FDA UDI
Generic Name
Pulse oximetry telemetric monitoring system transmitter FDA UDI
Model / Reference
3715 FDA UDI

Identifiers

Primary DI / UDI-DI
00843997008259 FDA UDI
FDA Product Code
MSX FDA UDI
GMDN Term
Pulse oximetry telemetric monitoring system transmitter 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulse oximetry telemetric monitoring system transmitter

MyView™ Presence Tag by Masimo Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximetry telemetric monitoring system transmitter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Masimo Corporation

Sources (1)

  • FDA UDI fef261ae-5f93-4893-b477-c432a37fa605 33 fields · synced May 30, 2026