Data / Medical devices / Filter, Bacterial, Breathing-Circuit / Mexico
FDA-registered makers of Filter, Bacterial, Breathing-Circuit in Mexico: 16 establishments
16 establishments in Mexico are registered with the FDA to make Filter, Bacterial, Breathing-Circuit (product code CAH). 10 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Filter, Bacterial, Breathing-Circuit
- Product code
- CAH
- Country
- Mexico
Makers of Filter, Bacterial, Breathing-Circuit in Mexico
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| ICU Medical Healthcare Manufacturing S.A. de C.V. | Tijuana, B.C. C.P. Baja California, Mexico | Manufacturer | 5 | May 13, 2004 | 0 | 0 | 0 | api.fda.gov |
| WESTMED de Mexico, S.A de C.V. | Tecate Baja California, Mexico | Contract manufacturer, Manufacturer, Repackager or relabeler | 4 | December 6, 2012 | 0 | 0 | 0 | api.fda.gov |
| Westmed Javid de Mexico, S.A. de C.V. | NOGALES Sonora, Mexico | Contract manufacturer, Manufacturer | 4 | December 6, 2012 | 0 | 0 | 0 | api.fda.gov |
| Productos Medline S.A. De C.V. | NUEVO LAREDO Tamaulipas, Mexico | Manufacturer, Repackager or relabeler | 2 | August 1, 2002 | 0 | 0 | 0 | api.fda.gov |
| S & Mohr America, S.A. DE C.V. | ESTADO DE MEXICO Ciudad de Mexico, Mexico | Manufacturer | 2 | March 16, 2020 | 0 | 1 | 0 | api.fda.gov |
| GVS Filter Technology De Mexico | Apodaca N.L Nuevo Leon, Mexico | Manufacturer | 1 | May 13, 2004 | 0 | 0 | 0 | api.fda.gov |
| IVEMSA S.A. de C.V DIVISION AG INDUSTRIES | Tijuana Baja California, Mexico | Manufacturer | 1 | December 14, 2005 | 0 | 0 | 0 | api.fda.gov |
| Medline Soluciones Medicas | Nuevo Laredo Tamaulipas, Mexico | Manufacturer, Repackager or relabeler | 1 | January 26, 1993 | 0 | 0 | 0 | api.fda.gov |
| Productos Urologos De Mexico S.A. De C.V. | MEXICALI Baja California, Mexico | Contract manufacturer, Manufacturer | 1 | April 5, 1985 | 0 | 0 | 0 | api.fda.gov |
| Teleflex Medical de Tecate, S. de R.L de C.V. | TECATE Baja California, Mexico | Manufacturer | 1 | April 15, 1997 | 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 | |
| Haemotronic De Mexico S De RL | REYNOSA Tamaulipas, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ICU Medical Healthcare Manufacturing S.A. de C.V. | APODACA Nuevo Leon, Mexico | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Integra Biotechnical, SA de CV | Tijuana Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Teleflex Medical de Mexico, S. de R.L. de C.V. | NUEVO LAREDO Tamaulipas, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Westmed de Mexico, S.A de C.V | NOGALES 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.