Primary Device ID | 00821684046869 |
NIH Device Record Key | 55ea24c3-1ff2-4e31-a795-81dd5dc51089 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PowerCross |
Version Model Number | AB18W060060150 |
Catalog Number | AB18W060060150 |
Company DUNS | 968903703 |
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 | |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Outer Diameter | 6 Millimeter |
Length | 60 Millimeter |
Catheter Gauge | 5 French |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00821684046869 [Primary] |
LIT | Catheter, angioplasty, peripheral, transluminal |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-08-09 |
Device Publish Date | 2015-10-09 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
POWERCROSS 86434077 4872927 Live/Registered |
Covidien, LP 2014-10-24 |
POWERCROSS 76065051 2538651 Dead/Cancelled |
EIDER 2000-06-07 |
POWERCROSS 76065051 2538651 Dead/Cancelled |
Bibollet, Jean Claude 2000-06-07 |