Multifire Endo TA 010903

GUDID 10884521047754

Stapler

Covidien LP

Endoscopic manual linear cutting stapler, single-use

• Primary Device ID: 10884521047754
• NIH Device Record Key: ece3cf7f-0468-4dd2-90d1-569b18ff3a5e
• Commercial Distribution Discontinuation: 2019-10-02
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Multifire Endo TA
• Version Model Number: 010903
• Catalog Number: 010903
• 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

Device Dimensions

• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter
• Height: 3.5 Millimeter
• Length: 30 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521047754 [Primary]
GS1	20884521047751 [Package]; Package: CASE [3 Units]; Discontinued: 2019-10-02; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K910192

FDA Product Code

• GDW: STAPLE, IMPLANTABLE

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: 2023-09-21
• Device Publish Date: 2015-05-25

On-Brand Devices [Multifire Endo TA]

• 20884521047775: Loading Unit
• 20884521047768: Loading Unit
• 20884521047744: Stapler
• 10884521047754: Stapler