Versaport 177801

GUDID 10884521078543

Reusable Cannula

Covidien LP

Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable Laparoscopic access cannula, reusable
Primary Device ID10884521078543
NIH Device Record Keyc8180ec9-577a-4fef-867e-1e3608e7cb14
Commercial Distribution Discontinuation2020-09-03
Commercial Distribution StatusNot in Commercial Distribution
Brand NameVersaport
Version Model Number177801
Catalog Number177801
Company DUNS058614483
Company NameCovidien LP
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com

Device Dimensions

Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0
Outer Diameter5 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110884521078543 [Primary]
GS110884521078543 [Primary]
GS110884521078543 [Primary]
GS110884521078543 [Primary]
GS110884521078543 [Primary]
GS110884521078543 [Primary]
GS110884521078543 [Primary]
GS110884521078543 [Primary]
GS110884521078543 [Primary]
GS110884521078543 [Primary]
GS110884521078543 [Primary]
GS110884521078543 [Primary]
GS110884521078543 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery
GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2020-09-15
Device Publish Date2016-09-24

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10884521078543Reusable Cannula
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