| Primary Device ID | 03596010610263 |
| NIH Device Record Key | 79aac0f8-7b66-4181-8f54-e2baf960e409 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CROSSTRAC |
| Version Model Number | 72201727 |
| Catalog Number | 72201727 |
| Company DUNS | 109903521 |
| Company Name | Smith & Nephew, 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03596010610263 [Primary] |
| NBH | ACCESSORIES,ARTHROSCOPIC |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
[03596010610263]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-31 |
| Device Publish Date | 2015-08-29 |
| 00885554022223 | MTO ASSEMBLY BULLET CROSSTRAC II |
| 00885554022216 | MTO ASSEMBLY HIP GUIDE CROSSTRAC II |
| 03596010610270 | TRAY CROSSTRAC |
| 03596010610263 | CROSSTRAC HIP GUIDE BULLET |
| 03596010610256 | CROSSTRAC HIP GUIDE |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CROSSTRAC 79136130 4496741 Live/Registered |
Continental Reifen Deutschland GmbH 2013-07-29 |
![]() CROSSTRAC 77378549 3548045 Dead/Cancelled |
Smith & Nephew, Inc. 2008-01-23 |