Ventricular vent catheter

GUDID 10803622106320

LIVANOVA USA, INC.

Heart ventricle cannula
Primary Device ID10803622106320
NIH Device Record Key4543a055-fa90-42ad-9ed5-2ae77c6bc135
Commercial Distribution StatusIn Commercial Distribution
Brand NameVentricular vent catheter
Version Model NumberVT-xxxxx
Company DUNS080914995
Company NameLIVANOVA USA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100803622106323 [Primary]
GS110803622106320 [Package]
Contains: 00803622106323
Package: CASE [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DWFCATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-08-15
Device Publish Date2015-07-16

On-Brand Devices [Ventricular vent catheter]

10803622106498VT-xxxxx
10803622106481VT-xxxxx
10803622106474VT-xxxxx
10803622106467VT-xxxxx
10803622106450VT-xxxxx
10803622106443VT-xxxxx
10803622106436VT-xxxxx
10803622106429VT-xxxxx
10803622106412VT-xxxxx
10803622106405VT-xxxxx
10803622106399VT-xxxxx
10803622106382VT-xxxxx
10803622106375VT-xxxxx
10803622106368VT-xxxxx
10803622106351VT-xxxxx
10803622106344VT-xxxxx
10803622106337VT-xxxxx
10803622106320VT-xxxxx

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