Primary Device ID | 00885554022216 |
NIH Device Record Key | ceb9093f-ebd6-4c0f-bd16-238df3273a5b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CROSSTRAC |
Version Model Number | 72203251 |
Catalog Number | 72203251 |
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 | |
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 | 00885554022216 [Primary] |
NBH | ACCESSORIES,ARTHROSCOPIC |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
Moist Heat or Steam Sterilization
[00885554022216]
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 |