| Primary Device ID | 00643169089600 |
| NIH Device Record Key | 9fcf73ad-54d7-4d84-a3eb-61bc63d6db1b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NavLock |
| Version Model Number | 9733734 |
| Company DUNS | 835233107 |
| Company Name | MEDTRONIC NAVIGATION, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169089600 [Primary] |
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00643169089600]
Moist Heat or Steam Sterilization
[00643169089600]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-08-09 |
| Device Publish Date | 2018-01-21 |
| 00643169101968 | TRACKER 9734734 NavLock UNIVERSAL GREEN |
| 00643169089600 | HANDLE 9733734 RATCHETING QC SM STRGHT |
| 00763000231835 | NAVLOCK KIT 9736060K BLACK |
| 00763000231521 | NAVLOCK KIT 9736061K BLUE |
| 00763000123185 | NAVLOCK 9736061 BLUE |
| 00763000123178 | NAVLOCK 9736060 BLACK |
| 00763000054465 | HANDLE 9733734 RATCHETING QC SM STRGHT |
| 00763000054489 | TRACKER 9734734 NavLock UNIVERSAL GREEN |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NAVLOCK 77824714 3848828 Live/Registered |
Medtronic Navigation, Inc. 2009-09-11 |