miniARM® multiSTATION™ System 081581

GUDID 00850012846321

BITA RetroSterno™ Paddle

LSI Solutions, Inc.

Surgical retractor/retraction system blade, reusable

• Primary Device ID: 00850012846321
• NIH Device Record Key: 6ebd7aa3-dc89-4348-af0a-0973bd1a61ad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: miniARM® multiSTATION™ System
• Version Model Number: 081581
• Catalog Number: 081581
• Company DUNS: 603420183
• Company Name: LSI Solutions, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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(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	00850012846321 [Primary]

FDA Product Code

• MDM: INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

Sterilization

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

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

[00850012846321]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-11
• Device Publish Date: 2024-01-03

On-Brand Devices [miniARM® multiSTATION™ System]

• 00850012846185: RetroSterno™ PADDLE KIT (1 each LIMA and RIMA RetroSterno™ Paddle)
• 00850012846178: RIMA RetroSterno™ PADDLE
• 00850012846161: LIMA RetroSterno™ PADDLE
• 00850012846154: SubX™ STERNAL ASCENDER™ SYSTEM
• 00850012846147: M55™ RIGID miniARM® HOLDER
• 00850012846321: BITA RetroSterno™ Paddle