Mi-CHORD™ 032150

GUDID 10850012846045

Mi-CHORD™ SYSTEM

LSI Solutions, Inc.

Suturing unit, single-use

• Primary Device ID: 10850012846045
• NIH Device Record Key: 5b7bc8fd-abc5-4e86-bff6-544c1da63f35
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mi-CHORD™
• Version Model Number: 032150
• Catalog Number: 032150
• Company DUNS: 603420183
• Company Name: LSI Solutions, Inc.
• 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(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850012846048 [Primary]
GS1	10850012846045 [Package]; Contains: 00850012846048; Package: Case [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• deNovo: DEN230069

FDA Product Code

• SBK: Artificial chordae tendineae surgical replacement system

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-07-22
• Device Publish Date: 2024-07-12

Devices Manufactured by LSI Solutions, Inc.

• 10850012846045 - Mi-CHORD™: 2024-07-22Mi-CHORD™ SYSTEM
• 10850012846045 - Mi-CHORD™: 2024-07-22 Mi-CHORD™ SYSTEM
• 10850012846342 - RAPORT™: 2024-05-30 RAPORT™ KIT
• 10850012846335 - PROSTAGRIP™: 2024-04-29 PROSTAGRIP™ DEVICE
• 10850012846281 - VIRTUOSEW™: 2024-02-22 VIRTUOSEW™ DEVICE
• 10850012846298 - AVR NAVIGATOR™: 2024-02-12 AVR NAVIGATOR™ SMALL RETRACTOR WITH DELIVERY DEVICE
• 10850012846304 - AVR NAVIGATOR™: 2024-02-12 AVR NAVIGATOR™ MEDIUM RETRACTOR WITH DELIVERY DEVICE
• 10850012846311 - AVR NAVIGATOR™: 2024-02-12 AVR NAVIGATOR™ LARGE RETRACTOR WITH DELIVERY DEVICE
• 00850012846321 - miniARM® multiSTATION™ System: 2024-01-11 BITA RetroSterno™ Paddle