Hancock™ II
GUDID 00763000318413
OBTURATOR 7505SET HK II AORTIC 26L CE
MEDTRONIC 3F THERAPEUTICS, INC.
Heart valve sizer, reusable| Primary Device ID | 00763000318413 |
| NIH Device Record Key | ee373c39-b5ee-4c9d-96a0-a52ad37a4fbe |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Hancock™ II |
| Version Model Number | 7505SET |
| Company DUNS | 079527232 |
| Company Name | MEDTRONIC 3F THERAPEUTICS, 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 |
Customer Support Contacts
Device Dimensions
| 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 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 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 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 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 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000318413 [Primary] |
FDA Product Code
| DTI | SIZER, HEART-VALVE, PROSTHESIS |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[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
[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 Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-04-12 |
| Device Publish Date | 2021-04-04 |
On-Brand Devices [Hancock™ II]
| 00763000318420 | OBTURATOR 7510SET HK II MITRAL 26L CE |
| 00763000318413 | OBTURATOR 7505SET HK II AORTIC 26L CE |
Trademark Results [Hancock]
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 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.