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LNCS® Pdtx SpO2 Pediatric Pulse Oximeter Adhesive Sensor

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 1860

by Masimo Corporation

Identity

Trade Name
LNCS Pdtx EUDAMED
LNCS® Pdtx SpO2 Pediatric Pulse Oximeter Adhesive Sensor FDA UDI
M-LNCS Pdtx pediatric adhesive sensor FDA UDI
Generic Name
Pulse oximeter probe, single-use FDA UDI
Device Name
LNCS SET Disposable Sensors EUDAMED
LNCS Pdtx SpO2 Pediatric Pulse Oximeter Adhesive Sensor FDA UDI
Model / Reference
1860 EUDAMEDFDA UDI
2909-5 FDA UDI
Description
LNCS Pdtx SpO2 Pediatric Pulse Oximeter Adhesive Sensor FDA UDI

Identifiers

Catalog Number
1860 FDA UDI
Primary DI / UDI-DI
10843997000458 EUDAMEDFDA UDI
10843997004722 FDA UDI
Basic UDI-DI
084399700000Z1T1B04V100G3 EUDAMED
Unit of Use DI
00843997000451 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 UDIFDA 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

LNCS® Pdtx SpO2 Pediatric 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 (3)

  • FDA UDI 9fe2fdc0-bab3-436e-a228-50f370bc82c7 37 fields · synced Jul 18, 2026
  • FDA UDI 1ac766e2-7f3c-4084-a0fd-3df7456b7ecb 33 fields · synced May 29, 2026
  • EUDAMED 0e0af1c6-949c-4f34-864d-013e86b585c4 61 fields · synced Jul 18, 2026