RD® QUICK LOAD® 023387

GUDID 10850012846526

RD® QUICK LOAD® SUTURE, 2-0 MONOGLIDE® DUO

LSI Solutions, Inc.

Polyester suture, non-bioabsorbable, multifilament

• Primary Device ID: 10850012846526
• NIH Device Record Key: 02a81f6d-b39a-46a8-a713-293a0ef4e571
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RD® QUICK LOAD®
• Version Model Number: 023387
• Catalog Number: 023387
• Company DUNS: 603420183
• Company Name: LSI Solutions, Inc.
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850012846529 [Primary]
GS1	10850012846526 [Package]; Contains: 00850012846529; Package: Inner Pack [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K031443

FDA Product Code

• NEW: Suture, surgical, absorbable, polydioxanone

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: 2025-07-17
• Device Publish Date: 2025-07-09

On-Brand Devices [RD® QUICK LOAD®]

• 10850200006312: RD® QUICK LOAD® SUTURE - 2-0 Polypropylene, Sterile, Synthetic, Non-Absorbable, Monofilament,
• 10850200006190: RD® QUICK LOAD® SUTURE - 0 MONOGLIDE®, Sterile, Synthetic, Polydioxanone, Absorbable, Monofil
• 10850200006183: RD® QUICK LOAD® SUTURE - 2-0 MONOGLIDE®, Sterile, Synthetic, Polydioxanone, Absorbable, Monof
• 10850200006176: RD® QUICK LOAD® SUTURE - 2-0 STRONGSORB®, Sterile, Synthetic, Polyglycolic Acid, Absorbable,
• 00850200006162: RD® QUICK LOAD® SUTURE - 0 Polyester, Sterile, Synthetic, Non-Absorbable, Coated, Braided, Sur
• 10850200006145: RD® QUICK LOAD® SUTURE - 2-0 Polyester, Sterile, Synthetic, Non-Absorbable, Coated, Braided, S
• 10850012846526: RD® QUICK LOAD® SUTURE, 2-0 MONOGLIDE® DUO