SCHILLER
Ecg, cardiopulmonary diagnostics and patient monitoring devices.
SCHILLER manufactures ECG, cardiopulmonary diagnostics and patient monitoring devices from its Baar operations. The company supplies healthcare systems, laboratories, OEM partners or regulated export customers across its listed primary markets.
- Type
- brand seeking distribution
- Location
- Baar, Switzerland
- Founded
- 1974
- Website
- schiller.ch
- Categories
- Medical & Healthcare Supplies
- Markets
- Switzerland, United States, Germany, Japan
Verified facts
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- places-goods-on-market (green), checked 2026-08-21 Swissmedic, swissdamed register of Swiss and Liechtenstein economic operators for medical devices
- registered-manufacturer (green), checked 2026-08-21 Swissmedic, swissdamed register of Swiss and Liechtenstein economic operators for medical devices
- fda-registered (green), checked 2026-07-21 FDA
- sanctions-clear (green), checked 2026-07-21 OpenSanctions
- registry-active-global (green), checked 2026-07-21 Zefix (Swiss commercial registry)
- lei-lapsed (amber), checked 2026-07-21 GLEIF
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- FDA Registered FDA Establishment Registration
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)