Schiller AG
Active in EUDAMEDSwitzerlandfrom SRN EUDAMED FDA SRN CH-MF-000012722 FEI 3002808182
Schiller AG is a medical device manufacturer based in Switzerland, with 201 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II; EU Class IIa, I and IIb) as of 12 Nov 2026.
- Devices
- 201
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 147
- EUDAMED 78
- FDA 510(k) 14
- Device classes
- FDA Class II 122
- EU Class IIa 26
- EU Class I 25
- EU Class IIb 24
- FDA Class I 4
- Top EMDN categories
- Sites and related companies
- SCHILLER Medizintechnik GmbH authorised representative
- Identifiers
- EUDAMED SRN CH-MF-000012722
- FDA FEI 3002808182
- DUNS 480868538
At a glance
EU certificates
0 of 1 in force. 1 certificate has expired.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA establishment
- Authorised rep.
- SCHILLER Medizintechnik GmbHDE
What Schiller AG makes
Schiller AG manufactures reusable electrocardiographic lead sets, including standard and specialized variants for AHA and IEC standards, as well as ECG monitoring devices like the CARDIOVIT AT-1 G2. The company also produces non-invasive blood pressure (NIBP) cuffs and spirometry devices, such as the SPIROVIT SP-1 G2.
The portfolio includes devices classified as Class I, Class II, Class IIa, and Class IIb under regulatory frameworks. Products are listed in the EU’s eudamed registry and the FDA’s 510(k) database, reflecting compliance with European and U.S. medical device regulations. The manufacturer is based in Switzerland.
Catalogue
Search and filter all 201 devicesShowing 1-50 of 201
Company details
- EUDAMED SRN
- CH-MF-000012722
- FDA FEI number
- 3002808182
- DUNS number
- 480868538
- EU VAT number
- CHE-105.868.779
- EUDAMED status
- Active
- EUDAMED registered name
- SCHILLER AG
- EUDAMED abbreviated name
- SAG
- Registered address
- 68, Altgasse, 6341, Baar, Switzerland
- Website
- www.schiller.ch
- info@schiller.ch
- Phone
- +41 41 766 42 42
- PRRC contact
- Blandine Momo
EUDAMED certificates
1 certificate0 valid, 1 expiredMDR 1
TÜV SÜD Product Service GmbH 0123 1 certificate
- G10 041505 0132 Expired
Quality management system EU MDR
- Issued
- 22 Nov 2024
- Expires
- 11 Nov 2026
FDA establishments
- Schiller Corp. US
Frequently asked questions
How many devices does Schiller AG have in the registry?
The registry currently lists 201 devices for Schiller AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Schiller AG's devices?
Among its 50 most recently registered devices, Schiller AG has devices listed in EUDAMED (14 devices), FDA 510(k) (1 device) and FDA GUDID (44 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Schiller AG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Schiller AG's devices are Class I, Class IIa, Class IIb and Class II. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Schiller AG?
EUDAMED lists 1 certificate for Schiller AG (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 22 Nov 2024.
What are the newest devices from Schiller AG in the registry?
The most recently registered devices listed for Schiller AG include SCHILLER ECG D-SUB2 B 3.1/2.55 x10 IEC, SCHILLER ECG BWDSC C 1.1/0.75 x10 AHA DP, medilogFD and ECG RS P 2.87 x4 IEC.
Which FDA establishments are linked to Schiller AG?
1 FDA establishment is linked to Schiller AG in the registry; they are listed on the company page.