Endo Slide 174510

GUDID 20884521050362

Knot Pusher

Covidien LP

Suture knot pusher, single-use

• Primary Device ID: 20884521050362
• NIH Device Record Key: 81953843-e781-4c3d-a5a6-c159fc1f120e
• Commercial Distribution Discontinuation: 2020-09-03
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Endo Slide
• Version Model Number: 174510
• Catalog Number: 174510
• 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

Customer Support Contacts

• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521050365 [Primary]
GS1	20884521050362 [Package]; Contains: 10884521050365; Package: CASE [12 Units]; Discontinued: 2020-09-03; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K925149

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-09-28
• Device Publish Date: 2016-09-24

Devices Manufactured by Covidien LP

• 10884521829527 - Valleylab: 2024-10-11 FT10 Electrosurgical Generator
• 10884521829534 - Valleylab: 2024-10-11 FT10 Vessel Sealing Generator
• 30884521843527 - Ritus: 2024-09-24 Peritoneal Dialysis Catheter Tenckhoff, 2 Cuffs
• 20884521843735 - Ritus: 2024-09-24 Peritoneal Dialysis Catheter Swan Neck Curl Cath, 2 Cuffs Left
• 20884521843766 - Ritus: 2024-09-24 Peritoneal Dialysis Catheter Swan Neck Curl Cath, 2 Cuffs Right
• 20884521843827 - Ritus: 2024-09-24 Peritoneal Dialysis Catheter Curl Cath, 2 Cuffs
• 20884521843865 - Ritus: 2024-09-24 Peritoneal Dialysis Catheter Swan Neck Tenckhoff, 2 Cuffs Left
• 20884521843872 - Ritus: 2024-09-24 Peritoneal Dialysis Catheter Swan Neck Tenckhoff, 2 Cuffs Right