Primary Device ID | 10884521081215 |
NIH Device Record Key | 702d10aa-3774-41de-a253-b25bf647c889 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Thoracoport |
Version Model Number | 179308 |
Catalog Number | 179308 |
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 |
Outer Diameter | 5 Millimeter |
Outer Diameter | 5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10884521081215 [Package] Contains: 20884521081212 Package: CASE [12 Units] In Commercial Distribution |
GS1 | 20884521081212 [Primary] |
GCJ | Laparoscope, general & plastic surgery |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-24 |
10884521081239 | Soft Trocar |
10884521081222 | Soft Trocar |
10884521081215 | Soft Trocar |
10884521081208 | Trocar |
10884521081192 | Trocar |
10884521081185 | Trocar |
10884521081178 | Trocar |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() THORACOPORT 74196412 1778335 Live/Registered |
COVIDIEN LP 1991-08-20 |