Surgiwand II

GUDID 20884523000891

Suction and Irrigation Device with L-Hook Tip

Covidien LP

Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use Surgical irrigation/aspiration cannula, non-illuminating, single-use

• Primary Device ID: 20884523000891
• NIH Device Record Key: 63c9242b-031e-4779-adb2-f878686592d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Surgiwand II
• Version Model Number: 178091
• 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: false
• 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
• 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

• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter
• Outer Diameter: 5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884523000894 [Primary]
GS1	20884523000891 [Package]; Contains: 10884523000894; Package: CASE [3 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K961771

FDA Product Code

• GEI: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

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: 2021-02-03
• Device Publish Date: 2016-09-24

On-Brand Devices [Surgiwand II]

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• 20884523000921: Suction and Irrigation Device with Spatula Tip
• 20884523000914: Suction and Irrigation Device with Spatula Tip
• 20884523000907: Suction and Irrigation Device with L-Hook Tip
• 20884523000891: Suction and Irrigation Device with L-Hook Tip
• 20884523000884: Suction and Irrigation Device
• 20884523000877: Suction and Irrigation Device
• 20884523000860: Suction and Irrigation Device