AnastoPod™ 081420

GUDID 10850012846267

AnastoPod™ DEVICE

LSI Solutions, Inc.

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• Primary Device ID: 10850012846267
• NIH Device Record Key: e280454f-c73b-4035-8a13-54910cb42822
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AnastoPod™
• Version Model Number: 081420
• Catalog Number: 081420
• 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: 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
• 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	00850012846260 [Primary]
GS1	10850012846267 [Package]; Contains: 00850012846260; Package: Case [4 Units]; In Commercial Distribution

FDA Product Code

• MDM: INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

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: 2023-07-31
• Device Publish Date: 2023-07-21

Devices Manufactured by LSI Solutions, Inc.

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• 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
• 10850012846267 - AnastoPod™: 2023-07-31AnastoPod™ DEVICE
• 10850012846267 - AnastoPod™: 2023-07-31 AnastoPod™ DEVICE
• 10850012846007 - PNEUMOSTOP®: 2022-11-14 PNEUMOSTOP® DEVICE
• 10850012846014 - PNEUMOSTOP®: 2022-11-14 PNEUMOSTOP® PLUS DEVICE