Data / Medical devices / Ventilator, Non-Continuous (Respirator) / Mexico
FDA-registered makers of Ventilator, Non-Continuous (Respirator) in Mexico: 9 establishments
9 establishments in Mexico are registered with the FDA to make Ventilator, Non-Continuous (Respirator) (product code BZD). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Ventilator, Non-Continuous (Respirator)
- Product code
- BZD
- Country
- Mexico
Makers of Ventilator, Non-Continuous (Respirator) in Mexico
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Productos Urologos De Mexico S.A. De C.V. | MEXICALI Baja California, Mexico | Contract manufacturer, Manufacturer | 2 | February 13, 2004 | 0 | 0 | 0 | api.fda.gov |
| Covidien | TIJUANA, B.C. Mexico, Mexico | Manufacturer | 1 | September 6, 2000 | 0 | 0 | 0 | api.fda.gov |
| Covidien | Ciudad Juarez Chihuahua, Mexico | Manufacturer | 1 | September 6, 2000 | 0 | 0 | 0 | api.fda.gov |
| Fisher & Paykel Healthcare S.a.de C.V. | Tijuana, Baja California, Mexico | Contract manufacturer, Exporter to the US | 1 | December 22, 2006 | 0 | 0 | 0 | api.fda.gov |
| Rci Hudson De Mexico S. De RL. De CV. | Nuevo Laredo Tamaulipas, Mexico | Manufacturer | 1 | April 21, 1987 | 0 | 0 | 0 | api.fda.gov |
| AP Services de Mexico, S. De R.L. De C.V. | Tijuana Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fisher & Paykel Healthcare S.A.de C.V. | Tijuana Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Iimed Medical Mexicana S. De R.L. De C.V. | Reynosa Tamaulipas, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Velcromex, S.A. De C.V. | AGUA PRIETA Sonora, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.