Thoracoport 179310

GUDID 10884521081239

Soft Trocar

Covidien LP

Laparoscopic access cannula anchor, single-use Laparoscopic access cannula anchor, single-use

• Primary Device ID: 10884521081239
• NIH Device Record Key: 50b795b3-acf1-4ad2-9145-5c3ecc8155ee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Thoracoport
• Version Model Number: 179310
• Catalog Number: 179310
• 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

Device Dimensions

• Outer Diameter: 15 Millimeter
• Outer Diameter: 15 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521081239 [Package]; Contains: 20884521081236; Package: CASE [12 Units]; In Commercial Distribution
GS1	20884521081236 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K992288

FDA Product Code

• GCJ: Laparoscope, general & plastic surgery

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [Thoracoport]

• 10884521081239: Soft Trocar
• 10884521081222: Soft Trocar
• 10884521081215: Soft Trocar
• 10884521081208: Trocar
• 10884521081192: Trocar
• 10884521081185: Trocar
• 10884521081178: Trocar