Signia SIGPSHELL

GUDID 20884521543796

Power Shell

Covidien LP

Surgical stapler handpiece housing

• Primary Device ID: 20884521543796
• NIH Device Record Key: e7693ab4-f1b4-4f6b-b3e8-329c20cd1834
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Signia
• Version Model Number: SIGPSHELL
• Catalog Number: SIGPSHELL
• 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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *none

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521543799 [Primary]
GS1	20884521543796 [Package]; Contains: 10884521543799; Package: CASE [6 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K160176

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: 2019-07-19
• Device Publish Date: 2017-08-08

On-Brand Devices [Signia]

• 10884521543829: Linear Adapter Short
• 10884521543805: Linear Adapter
• 10884521543898: Sterilization Tray
• 10884521703704: Circular Adapter Reusable Trocar Tip Protector
• 10884521703698: Black Extra Thick Circular Adapter XL Length
• 10884521703681: Circular Adapter Standard Length
• 20884521543796: Power Shell
• 20884521741888: Small Diameter Curved Tip Intelligent Reload Vascular/Thin; For use with 8 mm Cannula or larger
• 20884521741871: Gray Small Diameter Curved Tip Intelligent Reload Vascular; For use with 8 mm Cannula or larger
• 20884521741840: Small Diameter Curved Tip Intelligent Reload Vascular/Thin; For use with 8 mm Cannula or larger
• 10884521543850: Four-Bay Smart Charger
• 10884521543867: Single-Bay Charger
• 10884521543782: Power Handle
• 10884521543812: Linear Adapter XL
• 10884521797437: Power Handle, Refurbished
• 20884521543505: Loading Unit
• 20884521543499: Loading Unit
• 10884521543874: Reusable Insertion Guide
• 10884521543881: Manual Retraction Tool