Seerlinq s.r.o.
Slovakia SK-MF-000040803 Last updated 17 Sep 2026
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- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
SEERLINQ HeartCore Ref 1
EUDAMED certificates
3EC International a.s. 2265 1 certificate
- 2025-MDR/QS-013/A Amended
Quality management system EU MDR
- Issued
- 17 Sep 2026
- Expires
- 7 Feb 2030
- Reason
- Mnf data change
Related companies
Notified bodies
About
The Seerlinq Telemedicine Service is a unique and simple solution for heart failure patients.
What Seerlinq s.r.o. makes
Seerlinq s.r.o. makes the SEERLINQ HeartCore device, which is a telemedicine solution for heart failure patients.
The SEERLINQ HeartCore is classified as a Class IIb medical device and is listed in the EUDAMED database; the company is based in Slovakia.
Frequently asked questions
What does Seerlinq s.r.o. make?
Seerlinq s.r.o. makes the SEERLINQ HeartCore device, which is a telemedicine solution designed for heart failure patients, as stated in the provided summary.
Where is Seerlinq s.r.o. based?
Seerlinq s.r.o. is based in Slovakia, as indicated by the country code SK in the device data.
Which regulatory registry lists Seerlinq s.r.o.'s devices?
The SEERLINQ HeartCore device made by Seerlinq s.r.o. is listed in the EUDAMED database, which is the European Union's medical device registry.
How is the SEERLINQ HeartCore device classified?
The SEERLINQ HeartCore device is classified as a Class IIb medical device, according to the device class information provided in the data.
Information
- Country
- Slovakia
- Address
- 160/14, Pekárska , Trnava, Slovakia
- Website
- seerlinq.com
- linkedin.com/company/seerlinq
- [email protected]
- Phone
- +421 2/222 009 95
- PRRC contact
- Štefan Karolčík
- EUDAMED SRN
- SK-MF-000040803