Quick Connect SpO2 Starter Kit

FDA UDI

Class II (US FDA UDI)

by Philips DS North America LLC

Identity

Trade Name: Quick Connect SpO2 Starter Kit FDA UDI
Generic Name: Pulse oximeter probe, single-use FDA UDI
Model / Reference: 989803167111 FDA UDI

Identifiers

Catalog Number: 989803167111 FDA UDI
Primary DI / UDI-DI: 00884838042476 FDA UDI
FDA Product Code: DQA FDA UDI
GMDN Term: Pulse oximeter probe, single-use 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Pulse oximeter probe, single-use

Quick Connect SpO2 Starter Kit by Philips DS North America LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Pulse oximeter probe, single-use.

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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 DS North America LLC

Sources (1)

FDA UDI c4bb5d2d-4d00-4fdd-87f1-d076204627e6 34 fields · synced Jun 8, 2026