IntelliVue CL SpO2 Pod

FDA UDI

Class II (US FDA UDI)

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name: IntelliVue CL SpO2 Pod FDA UDI
Generic Name: Pulse oximeter FDA UDI
Device Name: IntelliVue Cableless SpO2 Pod, a battery-powered pulse oximeter device for Cableless Monitoring of patients. The IntelliVue CL SpO2 Pod provides arterial oxygen saturation, pulse rate and pleth wave form via short range radio to the receiving system. FDA UDI
Model / Reference: IntelliVue CL SpO2 Pod FDA UDI
Description: IntelliVue Cableless SpO2 Pod, a battery-powered pulse oximeter device for Cableless Monitoring of patients. The IntelliVue CL SpO2 Pod provides arterial oxygen saturation, pulse rate and pleth wave form via short range radio to the receiving system. FDA UDI

Identifiers

Catalog Number: 865215 FDA UDI
Primary DI / UDI-DI: 00884838020665 FDA UDI
FDA Product Code: DRG FDA UDI
GMDN Term: Pulse oximeter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.2910 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Pulse oximeter

IntelliVue CL SpO2 Pod by Philips Medizin Systeme Böblingen GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Philips Medizin Systeme Böblingen GmbH

Sources (1)

FDA UDI db02e170-7265-48bc-8b7a-0ad253125685 36 fields · synced Jun 8, 2026