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External Pulse Oximeter (Nonin XPOD)

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
External Pulse Oximeter (Nonin XPOD) FDA UDI
Generic Name
Patient monitoring system module, pulse oximetry FDA UDI
Device Name
External Pulse Oximeter (Nonin XPOD) FDA UDI
Model / Reference
External Pulse Oximeter (Nonin XPOD) FDA UDI
Description
External Pulse Oximeter (Nonin XPOD) FDA UDI

Identifiers

Catalog Number
1129640 FDA UDI
Primary DI / UDI-DI
00606959052031 FDA UDI
FDA Product Code
NOU FDA UDI
CBK FDA UDI
DQA FDA UDI
GMDN Term
Patient monitoring system module, pulse oximetry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 FDA UDI
870.2700 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

No

FDA UDI

Category: Patient monitoring system module, pulse oximetry

External Pulse Oximeter (Nonin XPOD) by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient monitoring system module, pulse oximetry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI 2aa7a05d-cfbc-4a94-8030-f054099c3d45 35 fields · synced May 30, 2026