| Primary Device ID | 00763000318598 |
| NIH Device Record Key | 34d5d240-f4a2-4465-866f-28789db9cd64 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Medtronic Open Pivot™ |
| Version Model Number | 577 |
| 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 |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000318598 [Primary] |
| DTI | SIZER, HEART-VALVE, PROSTHESIS |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
[00763000318598]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-06-14 |
| Device Publish Date | 2021-06-06 |
| 00763000318581 | HANDLE BENDABLE 569 OPHV 26L CE |
| 00763000318604 | SIZER SET 578 OPHV AP-AP360 NITINOL26LCE |
| 00763000318598 | SIZER SET 577 OPHV STANDARD 26L CE |
| 00763000318550 | SIZER SET 576 OPHV NITINOL 26L CE |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEDTRONIC OPEN PIVOT 85760168 4645652 Live/Registered |
Medtronic, Inc. 2012-10-22 |
![]() MEDTRONIC OPEN PIVOT 85752964 not registered Dead/Abandoned |
Medtronic, Inc. 2012-10-12 |