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Sentri, Adult, Nasal Cannula with Curved Prongs, CO2 Monitoring Line 1144017

by Intersurgical Incorporated

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05030267159802 UDI-DI Date16 May 2023ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Sentri, Adult, Nasal Cannula with Curved Prongs, CO2 Monitoring Line
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling
Model / Reference
1144017
Primary DI / UDI-DI
05030267159802
FDA Product Code
CCK
GMDN Term
Nasal oxygen cannula, carbon-dioxide-sampling
Device Class
Class II
Regulation Number
868.1400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Nasal oxygen cannula, carbon-dioxide-sampling

Cleared under the same submission (K122075)

Other devices from Intersurgical Incorporated

See all devices from Intersurgical Incorporated →

Properties

  • Single Use
  • Prescription Use
  • Combination Product
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

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