Endo Slide 174510

GUDID 20884521050362

Knot Pusher

Covidien LP

Suture knot pusher, single-use
Primary Device ID20884521050362
NIH Device Record Key81953843-e781-4c3d-a5a6-c159fc1f120e
Commercial Distribution Discontinuation2020-09-03
Commercial Distribution StatusNot in Commercial Distribution
Brand NameEndo Slide
Version Model Number174510
Catalog Number174510
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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
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 Identifiers

Device Issuing AgencyDevice ID
GS110884521050365 [Primary]
GS120884521050362 [Package]
Contains: 10884521050365
Package: CASE [12 Units]
Discontinued: 2020-09-03
Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, general & plastic surgery

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2023-09-28
Device Publish Date2016-09-24

Devices Manufactured by Covidien LP

20884521084992 - DAR2025-04-21 Catheter Mount
20884521842530 - DAR2025-04-21 Catheter Mount Extension Tube
20884521844770 - DAR2025-04-21 Catheter Mount Extendable Extension Tube
30884522019747 - DAR2025-04-21 Catheter Mount
30884522019754 - DAR2025-04-21 Catheter Mount
30884522019778 - DAR2025-04-21 Catheter Mount
30884522019785 - DAR2025-04-21 Catheter Mount
20884522019801 - DAR2025-04-21 Catheter Mount

Trademark Results [Endo Slide]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ENDO SLIDE
ENDO SLIDE
74308320 1860329 Live/Registered
COVIDIEN LP
1992-08-26

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