Skip to content

Portex 20-1112

by ICU Medical, Inc.

Portex 20-1112 is a Class II device made by ICU Medical, Inc., listed in FDA GUDID since 11 Oct 2016 (UDI-DI 10788942211124), 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 Number10788942211124 UDI-DI Date11 Oct 2016ListedStatusListed 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  • Withdrawn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
Incentive spirometer
Model / reference
20-1112
Primary DI / UDI-DI
10788942211124
FDA product code
BWF
GMDN term
Incentive spirometer
Device class
Class II
Regulation number
868.5690
GUDID distribution status
In Commercial Distribution

Related devices

Category: Incentive spirometer

Similar devices

Other devices filed under FDA product code BWF (SPIROMETER, THERAPEUTIC (INCENTIVE)).

Other devices from ICU Medical, Inc.

See all devices from ICU Medical, Inc. →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)