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Hudson Rci IPN044248

by Teleflex Incorporated

Hudson Rci IPN044248 (353471) is a Class I device made by Teleflex Incorporated, listed in FDA GUDID since 15 Sep 2018 (UDI-DI 04026704580781), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04026704580781 UDI-DI Date15 Sep 2018ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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
Anaesthesia breathing circuit, single-use
Model / Ref / Catalog
IPN044248, 353471
Primary DI / UDI-DI
04026704580781
FDA product code
CAI
GMDN term
Anaesthesia breathing circuit, single-use
Device class
Class I
Regulation number
868.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Anaesthesia breathing circuit, single-use

Similar devices in this category

Other devices filed under Anaesthesia breathing circuit, single-use.

Other devices from Teleflex Incorporated

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  • Arrow IPNB00827 Open recall

    Class II

See all devices from Teleflex Incorporated →

Properties

  • Single use
  • Contains latex
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)