FDA UDI In Commercial Distribution 🇺🇸 United States

Neo Legacy

DI: 00859144004210 · Model: 2100 · CVRX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Neo Legacy
Primary DI
00859144004210
Version / Model
2100
Catalog Number
100053-301
Company Name
CVRX, INC.
Labeler DUNS
052373680
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-01-21
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
85bc0832-5982-4728-bee0-016197cd9dd2

Device Description

Neo Legacy 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
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 00859144004210