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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

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20884838115389 UDI-DI Date16 Oct 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • 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  • Withdrawn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, 989803205381
Primary DI / UDI-DI
20884838115389
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

Other devices from Philips Medizin Systeme Böblingen GmbH

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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