Multifire Endo SGIA 030333

GUDID 10884523003758

Straight Knifeless Loading Unit

Covidien LP

Surgical staple loading unit, non-cutting

• Primary Device ID: 10884523003758
• NIH Device Record Key: 3ee2ffb4-90ba-4aab-8347-6617b4158e22
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Multifire Endo SGIA
• Version Model Number: 030333
• Catalog Number: 030333
• 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

• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter
• Height: 2.5 Millimeter
• Length: 30 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884523003758 [Primary]
GS1	20884523003755 [Package]; Package: CASE [12 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: 2015-05-25

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• 30884522020279 - DAR: 2025-03-18 Catheter Mount
• 10884522034753 - DAR: 2025-03-18 Catheter Mount Extendable
• 10884522034791 - DAR: 2025-03-18 Catheter Mount Extendable
• 20884521066172 - DAR: 2025-03-17 Catheter Mount Extendable
• 10884521528086 - DAR: 2025-03-17 Catheter Mount
• 20884522020081 - DAR: 2025-03-17 Catheter Mount