PERCEVAL

GUDID 00896208000443

Livanova Canada Corp

Aortic heart valve bioprosthesis Aortic heart valve bioprosthesis Aortic heart valve bioprosthesis Aortic heart valve bioprosthesis Aortic heart valve bioprosthesis Aortic heart valve bioprosthesis Aortic heart valve bioprosthesis Aortic heart valve bioprosthesis Aortic heart valve bioprosthesis Aortic heart valve bioprosthesis
Primary Device ID00896208000443
NIH Device Record Key9f983f94-560a-4dad-bc15-02e6c83fd7e0
Commercial Distribution StatusIn Commercial Distribution
Brand NamePERCEVAL
Version Model NumberPVS
Company DUNS243661431
Company NameLivanova Canada Corp
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
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 Identifiers

Device Issuing AgencyDevice ID
GS100896208000443 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LWRheart-valve, non-allograft tissue

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2021-02-05
Device Publish Date2016-02-25

On-Brand Devices [PERCEVAL]

00896208000443PVS
00896208000436PVS
00896208000429PVS
00896208000412PVS

Trademark Results [PERCEVAL]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PERCEVAL
PERCEVAL
79114598 4352084 Live/Registered
ATELIER PERCEVAL
2012-05-16
PERCEVAL
PERCEVAL
79083350 3919089 Live/Registered
SORIN GROUP ITALIA SRL
2010-03-22

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