Primary Device ID | 20884521099149 |
NIH Device Record Key | 7a16a481-5bef-4f53-8260-3b48229164bb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Chemosite |
Version Model Number | 120037 |
Catalog Number | 120037 |
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 | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Length | 19 Millimeter |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10884521099142 [Primary] |
GS1 | 20884521099149 [Package] Contains: 10884521099142 Package: CASE [20 Units] In Commercial Distribution |
LJT | PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2015-08-28 |
10884521099265 | Low Profile Venous Access System |
10884521099289 | Catheter Introducer Kit |
10884521099272 | Catheter Introducer Kit |
20884521099019 | Line Extension Set |
10884521176065 | Venous Access System |
20884521099194 | Straight Needle |
20884521099187 | Straight Needle |
20884521099170 | Straight Needle |
20884521099163 | Right Angle Needle |
20884521099156 | Right Angle Needle |
20884521099149 | Right Angle Needle |
20884521099132 | Right Angle Needle |
20884521099101 | Right Angle Needle |
20884521099071 | Line Extension Set |
20884521099064 | Line Extension Set,120075 |
20884521099057 | Line Extension Set |
20884521099040 | Line Extension Set |
20884521099033 | Line Extension Set |
20884521099026 | Line Extension Set |
20884521099002 | Line Extension Set |
20884521098999 | Line Extension Set |
10884521099401 | Low Profile Venous Access System |
10884521099395 | Low Profile Venous Access System |
10884521099388 | Low Profile Venous Access System |
10884521099371 | Low Profile Venous Access System |
10884521099364 | Low Profile Venous Access System,120027;120089 |
10884521099357 | Low Profile Venous Access System,120026;120039 |
10884521099340 | Low Profile Venous Access System |
10884521099333 | Venous Access System |
10884521099326 | Venous Access System,120039;120044 |
10884521099319 | Venous Access System |
10884521099302 | Venous Access System,120085;120089 |
10884521099296 | Venous Access System,120020;120039 |
10884521099258 | Low Profile Venous Access System |
10884521099241 | Venous Access System |
10884521099234 | Venous Access System |
10884521099203 | Venous Access System |
20884521099224 | Tunneler |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CHEMOSITE 75173830 2091327 Live/Registered |
COVIDIEN LP 1996-09-30 |