FDA UDI In Commercial Distribution 🇺🇸 United States

BAROSTIM NEO

DI: 00859144004432 · Model: 2102 · CVRX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BAROSTIM NEO
Primary DI
00859144004432
Version / Model
2102
Catalog Number
100054-202
Company Name
CVRX, INC.
Labeler DUNS
052373680
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-22
Public Version
1
Public Version Date
2019-08-30
Public Version Status
New
Public Device Record Key
eee607e1-731e-401b-935c-e1af1e4e674a

Device Description

BAROSTIM NEO Model 2102 Implantable Pulse Generator (US Commercial)

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
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 00859144004432

Customer Contacts

Phone
7634167457