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Oxygen Tubing with Connector, 7ft

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 Number00850057117455 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  • Withdrawn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
Oxygen administration tubing
Model / Ref / Catalog
Oxygen Tubing with Connector, 7ft, 91-101-US213
Primary DI / UDI-DI
00850057117455
510(k) Number
FDA Product Code
CBK
GMDN Term
Oxygen administration tubing
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
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

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