Data / Medical devices / Pump, Portable, Aspiration (Manual Or Powered) / Switzerland
FDA-registered makers of Pump, Portable, Aspiration (Manual Or Powered) in Switzerland: 5 establishments
5 establishments in Switzerland are registered with the FDA to make Pump, Portable, Aspiration (Manual Or Powered) (product code BTA). 3 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Pump, Portable, Aspiration (Manual Or Powered)
- Product code
- BTA
- Country
- Switzerland
Makers of Pump, Portable, Aspiration (Manual Or Powered) in Switzerland
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Medela AG | BAAR Zug, Switzerland | Complaint file establishment, Manufacturer | 9 | May 18, 2016 | 0 | 1 | 0 | api.fda.gov |
| Ardo Medical AG | UNTERAEGERI Zug, Switzerland | Manufacturer | 1 | June 8, 2001 | 0 | 0 | 0 | api.fda.gov |
| Nouvag AG | GOLDACH Sankt Gallen, Switzerland | Manufacturer | 1 | December 17, 2004 | 0 | 0 | 0 | api.fda.gov |
| Gebruder Renggli, AG | Schaffhausen, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Storz Endoskop Produktions GMBH | Schaffhausen, Switzerland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.