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Portex 66-2504

by ICU Medical, Inc.

Portex 66-2504 is a Class I device made by ICU Medical, Inc., listed in FDA GUDID since 2 Jul 2018 (UDI-DI 10788942625044), 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 Number10788942625044 UDI-DI Date2 Jul 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  • Withdrawn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
Portex
Generic name
Straight/elbow breathing circuit connector, reusable
Model / reference
66-2504
Primary DI / UDI-DI
10788942625044
FDA product code
BZA
GMDN term
Straight/elbow breathing circuit connector, reusable
Device class
Class I
Regulation number
868.5810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Straight/elbow breathing circuit connector, reusable

Similar devices in this category

Other devices filed under Straight/elbow breathing circuit connector, reusable.

Other devices from ICU Medical, Inc.

See all devices from ICU Medical, Inc. →

Properties

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