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RESPOND HME Patient Circuit Kit (Tubing, Connector & HME/

by Corvent Medical, Inc

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 Number00850057117417 UDI-DI Date6 Jan 2026ListedStatusListed 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  • Withdrawn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

Generic Name
Ventilator breathing circuit, single-use
Model / Ref / Catalog
RESPOND HME Patient Circuit Kit (Tubing, Connector & HME/, 91-101-US504
Primary DI / UDI-DI
00850057117417
510(k) Number
FDA Product Code
CBK
GMDN Term
Ventilator breathing circuit, single-use
Device Class
Class II
Regulation Number
868.5895
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K241135)

Show all (12)

Other devices from Corvent Medical, Inc

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Properties

  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No