ProSup TECG3004

GUDID 10884521177574

Pelvic Floor Repair Mesh,Polyester

SOFRADIM PRODUCTION

Pelvic organ prolapse surgical mesh, synthetic polymer

• Primary Device ID: 10884521177574
• NIH Device Record Key: 7581ae25-fbf8-4adb-adfb-ea9be47d5332
• Commercial Distribution Discontinuation: 2016-04-12
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ProSup
• Version Model Number: TECG3004
• Catalog Number: TECG3004
• Company DUNS: 576342646
• Company Name: SOFRADIM PRODUCTION
• 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

Device Dimensions

• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter
• Height: 4 Centimeter
• Width: 30 Centimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521177574 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K982532

FDA Product Code

• FTL: Mesh, surgical, polymeric

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: 2019-10-29
• Device Publish Date: 2015-10-06

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