Primary Device ID | 10884521514119 |
NIH Device Record Key | bb05a19b-aaf4-492d-977c-12578da93b92 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tritis |
Version Model Number | 2645SS |
Catalog Number | 2645SS |
Company DUNS | 058614483 |
Company Name | Covidien LP |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Length | 30 Millimeter |
Special Storage Condition, Specify | Between 0 and 0 *; |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10884521514119 [Primary] |
KMF | Bandage, liquid |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-06-07 |
Device Publish Date | 2018-07-29 |
10884521514133 | Nitinol Guide Wire |
10884521513983 | Tibial Tunnel Length Gauge |
10884521513952 | Inserter Stylus |
10884521513907 | Graft Dilator |
10884521514126 | Non Absorbable ACL Tibial Fixation System |
10884521514119 | Non Absorbable ACL Tibial Fixation System |
10884521514027 | Fixation Screw Driver |
10884521514010 | Implant Removal Tool |
10884521514003 | Hand Instrument Removal Tool |
10884521513990 | Graft Dilator |
10884521513945 | Graft Cleat Inserter |
10884521513938 | Inserter Stylus |
10884521513921 | Inserter Collet |
10884521513914 | Graft Dilator |
10884521513891 | Graft Dilator |
10884521513884 | Graft Dilator |
10884521513877 | ACL Tibial Reconstruction System Kit |
10884521514102 | Non Absorbable ACL Tibial Fixation System |
10884521514096 | Non Absorbable ACL Tibial Fixation System |
10884521514089 | Non Absorbable ACL Tibial Fixation System |
10884521514072 | Non Absorbable ACL Tibial Fixation System |
10884521514065 | Non Absorbable ACL Tibial Fixation System |
10884521514058 | Non Absorbable ACL Tibial Fixation System |
10884521514034 | Non Absorbable ACL Tibial Fixation System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRITIS 78689268 3172550 Live/Registered |
COVIDIEN LP 2005-08-10 |