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MedSource Pediatric Pulse Ox Sensor

FDA UDI

Class II (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource Pediatric Pulse Ox Sensor FDA UDI
Generic Name
Pulse oximeter probe, reprocessed FDA UDI
Device Name
Pediatric Pulse Ox Sensor FDA UDI
Model / Reference
MS-74011P FDA UDI
Description
Pediatric Pulse Ox Sensor FDA UDI

Identifiers

Primary DI / UDI-DI
00816703021446 FDA UDI
FDA Product Code
DQA FDA UDI
GMDN Term
Pulse oximeter probe, reprocessed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Category: Pulse oximeter probe, reprocessed

MedSource Pediatric Pulse Ox Sensor by Medsource International Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter probe, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0339dbfa-d0ea-46cd-add3-518a8ba12b5b 33 fields · synced May 30, 2026