Medex 22-2000
Medex 22-2000 is a Class II device made by ICU Medical, Inc., listed in FDA GUDID since 11 Oct 2016 (UDI-DI 10788942220003), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10788942220003 | Date11 Oct 2016 | StatusListed |
Official records
- AccessGUDID record 10788942220003
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Medex
- Generic name
- Incentive spirometer
- Model / reference
- 22-2000
- Primary DI / UDI-DI
- 10788942220003
- FDA product code
- BWF
- GMDN term
- Incentive spirometer
- Device class
- Class II
- Regulation number
- 868.5690
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code BWF (SPIROMETER, THERAPEUTIC (INCENTIVE)).
- VOLUREX II by Dhd Medical Products Div. Diemolding Corp.
- ROADRUNNER, PEP THERAPY DEVICE by Dhd Healthcare Corp.
- AIRLIFE ELECTRONIC INCENTIVE SPIROMETER by American Pharmaseal Div. Ahsc
- THE LUNG GYM (XLATOR AND NLATOR) by El-Fax Company, Inc.
- SPI-RISE by Certified Respiratory Services, Inc.
- Acapella Choice Blue Vibratory PEP Device by Smiths Medical
- VOLDYNE VOLUMETRIC INCENTIVE DEEP BR. EX by Chesebrough-Pond'S U.S.A. Co.
- VersaPAP Positive Airway Pressure (PAP) Device by TRUDELL MEDICAL INTERNATIONAL
- AEROSOL INHALATION MONITOR by Vitalograph, Ltd.
- PFLEX RESPIRATORY MUSCLE EXERCISER by Health Scan, Inc.