BAROSTIM NEO 100063-222

GUDID 00859144004470

BAROSTIM NEO Model 1037 Carotid Sinus Lead Kit

CVRX, INC.

Baroreceptor electrical stimulation system
Primary Device ID00859144004470
NIH Device Record Keyf4133b06-9448-4346-8bd8-5180edbe7289
Commercial Distribution StatusIn Commercial Distribution
Brand NameBAROSTIM NEO
Version Model Number1037
Catalog Number100063-222
Company DUNS052373680
Company NameCVRX, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7634167457
Emailacrouse@cvrx.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100859144004470 [Primary]

FDA Product Code

DSRStimulator, Carotid Sinus Nerve

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-08-30
Device Publish Date2019-08-22

On-Brand Devices [BAROSTIM NEO]

00859144004470BAROSTIM NEO Model 1037 Carotid Sinus Lead Kit
00859144004463BAROSTIM NEO Model 1036 Carotid Sinus Lead Kit (US Commercial)
00859144004432BAROSTIM NEO Model 2102 Implantable Pulse Generator (US Commercial)

Trademark Results [BAROSTIM NEO]

Mark Image

Registration | Serial
Company
Trademark
Application Date
BAROSTIM NEO
BAROSTIM NEO
85301899 4158924 Live/Registered
CVRx, Inc.
2011-04-22

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