ambIT* PIB-PCA v1.5 System w/Spike Filter Cass 220574

GUDID 00193494001308

ambIT* PIB-PCA v1.5 System w/Spike Filter Cass

Avanos Medical, Inc.

Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated Peripheral anaesthesia catheter set, non-medicated

• Primary Device ID: 00193494001308
• NIH Device Record Key: 02ee7d38-fd00-4eb0-a04e-45c673d57957
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ambIT* PIB-PCA v1.5 System w/Spike Filter Cass
• Version Model Number: 220574
• Catalog Number: 220574
• Company DUNS: 079375431
• Company Name: Avanos Medical, 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM
• Phone: +1(844)428-2667
• Email: PIQ@AVANOS.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00193494001308 [Primary]
GS1	10193494001305 [Package]; Package: CS [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162165

FDA Product Code

• FRN: Pump, infusion

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-03-07
• Device Publish Date: 2022-11-04

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