FDA UDI In Commercial Distribution 🇺🇸 United States

Barostim NEO2

DI: 00859144004623 · Model: 2104 · CVRX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Barostim NEO2
Primary DI
00859144004623
Version / Model
2104
Catalog Number
100065-202
Company Name
CVRX, INC.
Labeler DUNS
052373680
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-21
Public Version
1
Public Version Date
2026-01-29
Public Version Status
New
Public Device Record Key
dc7bbdb7-b609-4da9-9376-82b2e0c3326b

Device Description

Model 2104 Barostim NEO2 Implantable Pulse Generator

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DSR Stimulator, Carotid Sinus Nerve

GMDN Terms

Code Name
35369 Baroreceptor electrical stimulation system

Identifiers

Type ID
Primary 00859144004623

Customer Contacts

Phone
763-416-7457

Premarket Submissions

Submission Number Supplement Number
P180050 001