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22mm Duoflow B/System with Luer Connector Integral Mon Line and Elbow 1.8M 2920010

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 Number05030267157495 UDI-DI Date6 Oct 2025ListedStatusListed 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  • Withdrawn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
22mm Duoflow B/System with Luer Connector Integral Mon Line and Elbow 1.8M
Generic Name
Anaesthesia breathing circuit, reusable
Model / Reference
2920010
Primary DI / UDI-DI
05030267157495
FDA Product Code
CAI
GMDN Term
Anaesthesia breathing circuit, reusable
Device Class
Class I
Regulation Number
868.5240
GUDID distribution status
In Commercial Distribution

Other devices from Intersurgical Incorporated

See all devices from Intersurgical Incorporated →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No