Vercise™ Cartesia™

GUDID 08714729905271

30cm 8 Contact DBS Directional Lead Kit

BOSTON SCIENTIFIC NEUROMODULATION CORPORATION

Deep brain electrical stimulation system
Primary Device ID08714729905271
NIH Device Record Key6a1663c8-edaf-4769-9a8f-7c6c4e9075f4
Commercial Distribution StatusIn Commercial Distribution
Brand NameVercise™ Cartesia™
Version Model NumberDB-2202-30
Company DUNS824951958
Company NameBOSTON SCIENTIFIC NEUROMODULATION CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS108714729905271 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHLSTIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-11-03
Device Publish Date2019-01-20

On-Brand Devices [Vercise™ Cartesia™]

0871472990528845cm 8 Contact DBS Directional Lead Kit
0871472990527130cm 8 Contact DBS Directional Lead Kit

Trademark Results [Vercise]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VERCISE
VERCISE
85736351 4448879 Live/Registered
Boston Scientific Neuromodulation Corporation
2012-09-24
VERCISE
VERCISE
77385544 not registered Dead/Abandoned
Boston Scientific Neuromodulation Corporation
2008-01-31
VERCISE
VERCISE
77380935 not registered Dead/Abandoned
Advanced Bionics, LLC
2008-01-25

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.