Cvrx, Inc.
United States US-MF-000001082 Last updated 23 Oct 2026
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- Devices
- 17
- Registries
- EUDAMEDGUDIDFDA PMAFDA
- FDA recalls
- 0
Catalogue
Barostim™ Carotid Sinus Lead Ref 100063-211
Barostim NEO2 2104 Ref 2104
Barostim 9020 Ref 9020
Barostim™ Programmer System Ref 100067-201
Programmer System Ref 100055-201
Carotid Sinus Lead Repair Kit Ref 100056-201
Barostim Legacy Implantable Pulse Generator Ref 100053-201
Na 5500 Ref 5500
Neo Legacy 2100 Ref 2100
Barostim Neo 2102 Ref 2102
Barostim Neo 1037 Ref 1037
Na 5000 Ref 5000
BAROSTIM Lead Repair Kit 5010 Ref 5010
Barostim Neo 1036 Ref 1036
BAROSTIM Programmer 9010 Ref 9010
Na 5010 Ref 5010
Na 9010 Ref 9010
BAROSTIM NEO® System Ref P180050
EUDAMED certificates
Notified body 0050 2 certificates
- 745.059 Issued
Quality management system EU MDR
- Issued
- 30 Jun 2026
- Expires
- 8 Apr 2030
- TD745.059 Issued
Technical documentation EU MDR
- Issued
- 30 Jun 2026
- Expires
- 8 Apr 2030
Related companies
Notified bodies
- Notified body 0050
Information
- Country
- United States
- Address
- 9201, West Broadway Avenue, Minneapolis, Minnesota, United States
- Website
- www.barostim.com
- [email protected]
- Phone
- +1 763 416 2840
- PRRC contact
- Nikita Basandra
- EUDAMED SRN
- US-MF-000001082
- FDA FEI number
- 3007972010
- DUNS number
- 052373680