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MasimoSET® LNCS® Trauma SpO2 Adult Pulse Oximeter Adhesive Sensor

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 2411

by Masimo Corporation

Identity

Trade Name
LNCS Trauma Adult EUDAMED
MasimoSET® LNCS® Trauma SpO2 Adult Pulse Oximeter Adhesive Sensor FDA UDI
Generic Name
Pulse oximeter probe, single-use FDA UDI
Device Name
LNCS SET Disposable Sensors EUDAMED
MasimoSET LNCS Trauma SpO2 Adult Pulse Oximeter Adhesive Sensor FDA UDI
Model / Reference
2411 EUDAMEDFDA UDI
Description
MasimoSET LNCS Trauma SpO2 Adult Pulse Oximeter Adhesive Sensor FDA UDI

Identifiers

Catalog Number
2411 FDA UDI
Primary DI / UDI-DI
10843997002360 EUDAMEDFDA UDI
Basic UDI-DI
084399700000Z1T1B04V102G7 EUDAMED
Unit of Use DI
00843997002363 EUDAMED
510(k) Number
K101896 FDA UDI
FDA Product Code
DQA FDA UDI
EMDN Code
C900301 PULSE OXIMETER SENSORS EUDAMED
GMDN Term
Pulse oximeter probe, single-use FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pulse oximeter probe, single-use

MasimoSET® LNCS® Trauma SpO2 Adult Pulse Oximeter Adhesive Sensor by Masimo Corporation — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED

Similar devices

Also classified as Pulse oximeter probe, single-use.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Masimo Corporation

Sources (2)

  • FDA UDI 9fd4be67-a1f7-4d84-a972-4544d06c0811 37 fields · synced Oct 6, 2026
  • EUDAMED 60cf96d3-4cfc-4884-9c30-3c3e6b62c14e 61 fields · synced Aug 4, 2026