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Hudson Rci IPN044130

by Teleflex Incorporated 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number14026704610379 UDI-DI Date6 Nov 2018ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Hudson Rci
Generic Name
Nasal oxygen cannula, carbon-dioxide-sampling
Model / Ref / Catalog
IPN044130, 2857
Primary DI / UDI-DI
14026704610379
510(k) Number
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
MRI Safety
MR Unsafe

Other devices from Teleflex Incorporated

See all devices from Teleflex Incorporated →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number

Other properties (11)

  • 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
  • Manufacturing Date: No