Data / Medical devices / Filter, Bacterial, Breathing-Circuit / Taiwan
FDA-registered makers of Filter, Bacterial, Breathing-Circuit in Taiwan: 9 establishments
9 establishments in Taiwan are registered with the FDA to make Filter, Bacterial, Breathing-Circuit (product code CAH). 8 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
- Taiwan
Makers of Filter, Bacterial, Breathing-Circuit in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| BESMED HEALTH BUSINESS CORP.-Chiayi | Dalin Township Chiayi(County), Taiwan | Manufacturer | 1 | November 14, 2024 | 0 | 0 | 0 | api.fda.gov |
| Besmed Health Business Corporation | New Taipei City, Taiwan | Manufacturer | 1 | November 14, 2024 | 0 | 0 | 0 | api.fda.gov |
| Enchant Tek Co. Ltd. | Dongshan Township, Yilan County Taipei, Taiwan | Contract manufacturer, Exporter to the US | 1 | December 13, 2004 | 0 | 0 | 0 | api.fda.gov |
| Galemed Corp. | WU-JIA Yilan, Taiwan | Manufacturer | 1 | April 18, 2014 | 0 | 0 | 0 | api.fda.gov |
| Great Group Medical Co Ltd. | Changhua County, Taiwan | Exporter to the US, Manufacturer | 1 | March 27, 2022 | 0 | 0 | 0 | api.fda.gov |
| Hsiner Co., Ltd. | Taichung City, Taiwan | Exporter to the US, Manufacturer | 1 | July 24, 2009 | 0 | 0 | 0 | api.fda.gov |
| Hsiner Co., Ltd. | Taichung City, Taiwan | Exporter to the US, Manufacturer | 1 | July 24, 2009 | 0 | 0 | 0 | api.fda.gov |
| Kung Shin Plastics Co., Ltd. | New Taipei City, Taiwan | Exporter to the US, Manufacturer | 1 | September 20, 2004 | 0 | 1 | 0 | api.fda.gov |
| Saykia Corporation | Changhua County, Taiwan | 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.