Hancock™ II

GUDID 00763000318413

OBTURATOR 7505SET HK II AORTIC 26L CE

MEDTRONIC 3F THERAPEUTICS, INC.

Heart valve sizer, reusable
Primary Device ID00763000318413
NIH Device Record Keyee373c39-b5ee-4c9d-96a0-a52ad37a4fbe
Commercial Distribution StatusIn Commercial Distribution
Brand NameHancock™ II
Version Model Number7505SET
Company DUNS079527232
Company NameMEDTRONIC 3F THERAPEUTICS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
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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
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Device Size Text, specify0
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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
GS100763000318413 [Primary]

FDA Product Code

DTISIZER, HEART-VALVE, PROSTHESIS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


[00763000318413]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-04-12
Device Publish Date2021-04-04

On-Brand Devices [Hancock™ II]

00763000318420OBTURATOR 7510SET HK II MITRAL 26L CE
00763000318413OBTURATOR 7505SET HK II AORTIC 26L CE

Trademark Results [Hancock]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HANCOCK
HANCOCK
97024774 not registered Live/Pending
Lian,Yiqi
2021-09-13
HANCOCK
HANCOCK
90336626 not registered Live/Pending
DENG, XIAOMING
2020-11-23
HANCOCK
HANCOCK
88195550 5781071 Live/Registered
Hancock Concrete Products, LLC
2018-11-15
HANCOCK
HANCOCK
87434579 not registered Dead/Abandoned
631 SOUTH MAIN STREET DEVELOPMENT LLC
2017-05-03
HANCOCK
HANCOCK
86428532 not registered Dead/Abandoned
Hancock Holding Company
2014-10-20
HANCOCK
HANCOCK
85638797 4389753 Live/Registered
Hancock Concrete Products, LLC
2012-05-30
HANCOCK
HANCOCK
85600743 4340163 Dead/Cancelled
Thomas Hancock & Company Limited
2012-04-18
HANCOCK
HANCOCK
85433700 4248653 Live/Registered
Hancock Lumber Company, Inc.
2011-09-28
HANCOCK
HANCOCK
78607509 not registered Dead/Abandoned
Masco Corporation of Indiana
2005-04-13
HANCOCK
HANCOCK
78106915 2835369 Dead/Cancelled
NEWFREY LLC
2002-02-05
HANCOCK
HANCOCK
77750641 not registered Dead/Abandoned
Masco Retail Cabinet Group, LLC
2009-06-03
HANCOCK
HANCOCK
75013221 2126552 Dead/Cancelled
GLIDDEN COMPANY, THE
1995-11-01

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