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Sentri™ Intersurgical Ecolite™, Adult, Mask with Co Monitoring Line and Tube 1142035

by Intersurgical Incorporated

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05030267169634 UDI-DI Date21 Apr 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  • Withdrawn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

Trade Name
Sentri™ Intersurgical Ecolite™, Adult, Mask with Co Monitoring Line and Tube
Generic Name
Rebreathing oxygen face mask
Model / Reference
1142035
Primary DI / UDI-DI
05030267169634
FDA Product Code
CCK
GMDN Term
Rebreathing oxygen face mask
Device Class
Class II
Regulation Number
868.1400
GUDID distribution status
In Commercial Distribution

Other devices from Intersurgical Incorporated

See all devices from Intersurgical Incorporated →

Properties

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

Other properties (8)

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