Barostim NEO2 100065-202

GUDID 00859144004623

Baroreceptor electrical stimulation system

Primary Device ID	00859144004623
NIH Device Record Key	dc7bbdb7-b609-4da9-9376-82b2e0c3326b
Commercial Distribution Status	In Commercial Distribution
Brand Name	Barostim NEO2
Version Model Number	2104
Catalog Number	100065-202
Company DUNS	052373680
Company Name	CVRX, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	MR Conditional
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	false
Serial Number	true
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00859144004623 [Primary]

DSR	Stimulator, Carotid Sinus Nerve

Steralize Prior To Use	false
Device Is Sterile	true

00859144004623 - Barostim NEO2	2026-01-29Model 2104 Barostim NEO2 Implantable Pulse Generator
00859144004623 - Barostim NEO2	2026-01-29 Model 2104 Barostim NEO2 Implantable Pulse Generator
00859144004630 - Barostim	2026-01-29 Model 9020 Barostim Programmer System
00859144004432 - BAROSTIM NEO	2019-08-30 BAROSTIM NEO Model 2102 Implantable Pulse Generator (US Commercial)
00859144004449 - BAROSTIM Programmer	2019-08-30 Model 9010 Programmer System (US Commercial)
00859144004456 - BAROSTIM Lead Repair Kit	2019-08-30 Model 5010 Carotid Sinus Lead Repair Kit (US Commercial)
00859144004463 - BAROSTIM NEO	2019-08-30 BAROSTIM NEO Model 1036 Carotid Sinus Lead Kit (US Commercial)
00859144004470 - BAROSTIM NEO	2019-08-30 BAROSTIM NEO Model 1037 Carotid Sinus Lead Kit
00859144004128 - NA	2018-03-29 Programmer System

Mark Image Registration \| Serial	Company Trademark Application Date
BAROSTIM NEO2 90505451 not registered Live/Pending	CVRx, Inc. 2021-02-02