Primary Device ID | 00763000614041 |
NIH Device Record Key | 8a2301d2-264e-465d-9722-b54b7eb8ff34 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hancock™ II 7510 |
Version Model Number | 7510SET |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000614041 [Primary] |
DTI | SIZER, HEART-VALVE, PROSTHESIS |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00763000614041]
Moist Heat or Steam Sterilization
[00763000614041]
Moist Heat or Steam Sterilization
[00763000614041]
Moist Heat or Steam Sterilization
[00763000614041]
Moist Heat or Steam Sterilization
[00763000614041]
Moist Heat or Steam Sterilization
[00763000614041]
Moist Heat or Steam Sterilization
[00763000614041]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-11 |
Device Publish Date | 2025-03-03 |
00763000613617 - Mosaic™7308C | 2025-03-11 SIZERS 7308C MOSAIC CINCH AORTIC MDR |
00763000613624 - Mosaic Ultra™7308U | 2025-03-11 SIZERS 7308U MOSAIC ULTRA AORTIC MDR |
00763000613631 - Mosaic™7310 | 2025-03-11 OBTURATORS 7310 MOSAIC MITRAL MDR |
00763000613648 - NA | 2025-03-11 HANDLE 7639 VALVE MDR |
00763000613655 - NA | 2025-03-11 HANDLE 7639XL VALVE XL MDR |
00763000613662 - NA | 2025-03-11 ACCESSORY 7642 LOCK NUT MDR |
00763000614034 - Hancock™ II 7505 | 2025-03-11 OBTURATOR 7505SET HK II AORTIC MDR |
00763000614041 - Hancock™ II 7510 | 2025-03-11OBTURATOR 7510SET HK II MITRAL MDR |
00763000614041 - Hancock™ II 7510 | 2025-03-11 OBTURATOR 7510SET HK II MITRAL MDR |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() HANCOCK 97024774 not registered Live/Pending |
Lian,Yiqi 2021-09-13 |
![]() HANCOCK 90336626 not registered Live/Pending |
DENG, XIAOMING 2020-11-23 |
![]() HANCOCK 88195550 5781071 Live/Registered |
Hancock Concrete Products, LLC 2018-11-15 |
![]() HANCOCK 87434579 not registered Dead/Abandoned |
631 SOUTH MAIN STREET DEVELOPMENT LLC 2017-05-03 |
![]() HANCOCK 86428532 not registered Dead/Abandoned |
Hancock Holding Company 2014-10-20 |
![]() HANCOCK 85638797 4389753 Live/Registered |
Hancock Concrete Products, LLC 2012-05-30 |
![]() HANCOCK 85600743 4340163 Dead/Cancelled |
Thomas Hancock & Company Limited 2012-04-18 |
![]() HANCOCK 85433700 4248653 Live/Registered |
Hancock Lumber Company, Inc. 2011-09-28 |
![]() HANCOCK 78607509 not registered Dead/Abandoned |
Masco Corporation of Indiana 2005-04-13 |
![]() HANCOCK 78106915 2835369 Dead/Cancelled |
NEWFREY LLC 2002-02-05 |
![]() HANCOCK 77750641 not registered Dead/Abandoned |
Masco Retail Cabinet Group, LLC 2009-06-03 |
![]() HANCOCK 75013221 2126552 Dead/Cancelled |
GLIDDEN COMPANY, THE 1995-11-01 |