multiSTATION™ 080770

GUDID 00850012846352

DOC-X 25™ EXTENDER

LSI Solutions, Inc.

Surgical instrument assist arm system structural component

• Primary Device ID: 00850012846352
• NIH Device Record Key: 4e4eea09-2480-4f44-87f9-3a4534fc27b2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: multiSTATION™
• Version Model Number: 080770
• Catalog Number: 080770
• 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
• Phone: +1(866)575-3493
• Email: regulatorydpt@lsisolutions.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850012846352 [Primary]

FDA Product Code

• MDM: INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

Sterilization

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

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

[00850012846352]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-10-07
• Device Publish Date: 2024-09-27

On-Brand Devices [multiSTATION™]

• 00850012846369: DOC-X 45™ EXTENDER
• 00850012846352: DOC-X 25™ EXTENDER
• 00850012846253: DOC-X 15™ EXTENDER
• 00850012846376: 10mm COUPLER