Thoratec PVAD, Cannula Tunneler 20099-2575-001

GUDID 00813024013105

Thoratec Corporation

Vascular graft tunneller Vascular graft tunneller
Primary Device ID00813024013105
NIH Device Record Key1c3d497d-dd5a-4a0d-8699-d29800a71021
Commercial Distribution StatusIn Commercial Distribution
Brand NameThoratec PVAD, Cannula Tunneler
Version Model Number20099-2575-001
Catalog Number20099-2575-001
Company DUNS070156955
Company NameThoratec Corporation
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(855)478-5833
Emailcustomerservice@sjm.com
Phone+1(855)478-5833
Emailcustomerservice@sjm.com

Operating and Storage Conditions

Storage Environment TemperatureBetween 20 Degrees Celsius and 30 Degrees Celsius
Storage Environment TemperatureBetween 20 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100813024013105 [Primary]

FDA Product Code

DSQVentricular (Assisst) Bypass

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00813024013105]

Moist Heat or Steam Sterilization


[00813024013105]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2019-05-08
Device Publish Date2014-09-20

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