Multifire Endo GIA 030330L

GUDID 20884523003731

Straight Loading Unit

Covidien LP

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• Primary Device ID: 20884523003731
• NIH Device Record Key: 47cb0eee-9a11-478d-b832-92af05849317
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Multifire Endo GIA
• Version Model Number: 030330L
• Catalog Number: 030330L
• Company DUNS: 058614483
• Company Name: Covidien LP
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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
• Phone: +1(508)261-8000
• Email: covidien.udi@covidien.com

Device Dimensions

• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter
• Length: 30 Millimeter
• Height: 2 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884523003734 [Primary]
GS1	20884523003731 [Package]; Contains: 10884523003734; Package: CASE [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K900129

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: 5
• Public Version Date: 2019-05-07
• Device Publish Date: 2015-08-28

On-Brand Devices [Multifire Endo GIA]

• 20884523003779: Straight Loading Unit
• 20884523003762: Straight Loading Unit
• 20884523003748: Straight Stapler
• 20884523003731: Straight Loading Unit
• 20884523003793: Straight Stapler
• 20884523003786: Straight Stapler