Vessel Cannulae

GUDID 10803622106276

LIVANOVA USA, INC.

Cardioplegia cannula
Primary Device ID10803622106276
NIH Device Record Key62eac7cf-9c65-43f1-bbac-ca1d247250a3
Commercial Distribution StatusIn Commercial Distribution
Brand NameVessel Cannulae
Version Model NumberVC-xxxxx
Company DUNS080914995
Company NameLIVANOVA USA, 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 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
GS100803622106279 [Primary]
GS110803622106276 [Package]
Contains: 00803622106279
Package: CASE [20 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 [Vessel Cannulae]

10803622106313VC-xxxxx
10803622106306VC-xxxxx
10803622106290VC-xxxxx
10803622106283VC-xxxxx
10803622106276VC-xxxxx
10803622106269VC-xxxxx

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