Primary Device ID | 20884521180618 |
NIH Device Record Key | 9dabc3e1-9506-4841-8dcc-dec322bac11b |
Commercial Distribution Discontinuation | 2021-02-18 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Arthroport |
Version Model Number | 160202A |
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 | 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(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 | |
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 | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 8.6 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10884521180611 [Primary] |
GS1 | 20884521180618 [Package] Contains: 10884521180611 Package: CASE [6 Units] Discontinued: 2021-02-18 Not in Commercial Distribution |
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 | 4 |
Public Version Date | 2021-03-08 |
Device Publish Date | 2016-09-24 |
20884521180625 | Cannula System |
20884521180618 | Cannula System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ARTHROPORT 76450821 2826122 Live/Registered |
COVIDIEN LP 2002-09-13 |