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Oxygen Sensor OOMLF103

by Honeywell Healthcare Solutions GmbH

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04036616010801 UDI-DI Date3 Mar 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Oxygen Sensor
Generic name
Respiratory oxygen sensor
Model / Ref / Catalog
OOMLF103, E1002533
Primary DI / UDI-DI
04036616010801
FDA product code
CCL
GMDN term
Respiratory oxygen sensor
Device class
Class II
Regulation number
868.1720
GUDID distribution status
In Commercial Distribution
Size
Length — 247 Millimeter
Width — 150 Millimeter
Height — 30 Millimeter

Related devices

Category: Respiratory oxygen sensor

Other devices from Honeywell Healthcare Solutions GmbH

See all devices from Honeywell Healthcare Solutions GmbH →

Properties

  • Serial number
  • Manufacturing date

Other properties (13)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Lot / batch number: No
  • Expiration date: No