Nasal Alar SpO2 Sensor

by Philips Medizin Systeme Böblingen GmbH 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 2 Nov 2026. What this means

Regulatory status

as of registry sync 2 Nov 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number20884838115396 UDI-DI	Date16 Oct 2026Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name: Pulse oximeter probe, single-use
Model / Ref / Catalog: Nasal Alar SpO2 Sensor, 989803205391

Primary DI / UDI-DI: 20884838115396
FDA Product Code: DQA
GMDN Term: Pulse oximeter probe, single-use

Device Class: Class II
Regulation Number: 870.2700
GUDID distribution status: In Commercial Distribution

MRI Safety: MR Unsafe

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Properties

Single Use
Prescription Use
Lot / Batch Number
Expiration Date

Other properties (10)

Sterile: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Manufacturing Date: No